NAT8 c.428T>C ;(p.F143S)

Variant ID: 2-73868328-A-G

NM_003960.3(NAT8):c.428T>C;(p.F143S)

This variant was identified in 52 publications

View GRCh38 version.




Publications:


Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine.

Nature Genetics
Schlosser, Pascal P; Scherer, Nora N; Grundner-Culemann, Franziska F; Monteiro-Martins, Sara S; Haug, Stefan S; Steinbrenner, Inga I; Uluvar, Burulça B; Wuttke, Matthias M; Cheng, Yurong Y; Ekici, Arif B AB; Gyimesi, Gergely G; Karoly, Edward D ED; Kotsis, Fruzsina F; Mielke, Johanna J; Gomez, Maria F MF; Yu, Bing B; Grams, Morgan E ME; Coresh, Josef J; Boerwinkle, Eric E; Köttgen, Michael M; Kronenberg, Florian F; Meiselbach, Heike H; Mohney, Robert P RP; Akilesh, Shreeram S; , ; Schmidts, Miriam M; Hediger, Matthias A MA; Schultheiss, Ulla T UT; Eckardt, Kai-Uwe KU; Oefner, Peter J PJ; Sekula, Peggy P; Li, Yong Y; Köttgen, Anna A
Publication Date: 2023-06-05

Variant appearance in text: rs13538
PubMed Link: 37277652
Variant Present in the following documents:
  • 41588_2023_1409_MOESM4_ESM.pdf
  • 41588_2023_1409_MOESM5_ESM.pdf
View BVdb publication page



Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem
Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS
Publication Date: 2022-11

Variant appearance in text: NAT8: F143S; rs13538
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports
Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-10-14

Variant appearance in text: NAT8: F143S
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM15_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM3_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM10_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM9_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM13_ESM.xlsx, sheet 2
View BVdb publication page



Peptide ancestry informative markers in uterine neoplasms from women of European, African, and Asian ancestry.

Iscience
Bateman, Nicholas W NW; Tarney, Christopher M CM; Abulez, Tamara S TS; Hood, Brian L BL; Conrads, Kelly A KA; Zhou, Ming M; Soltis, Anthony R AR; Teng, Pang-Ning PN; Jackson, Amanda A; Tian, Chunqiao C; Dalgard, Clifton L CL; Wilkerson, Matthew D MD; Kessler, Michael D MD; Goecker, Zachary Z; Loffredo, Jeremy J; Shriver, Craig D CD; Hu, Hai H; Cote, Michele M; Parker, Glendon J GJ; Segars, James J; Al-Hendy, Ayman A; Risinger, John I JI; Phippen, Neil T NT; Casablanca, Yovanni Y; Darcy, Kathleen M KM; Maxwell, G Larry GL; Conrads, Thomas P TP; O'Connor, Timothy D TD
Publication Date: 2022-01-21

Variant appearance in text: NAT8: F143S; rs13538
PubMed Link: 35036865
Variant Present in the following documents:
  • mmc2.xlsx, sheet 1
View BVdb publication page



Prioritization of candidate genes for a South African family with Parkinson's disease using in-silico tools.

Plos One
Sebate, Boiketlo B; Cuttler, Katelyn K; Cloete, Ruben R; Britz, Marcell M; Christoffels, Alan A; Williams, Monique M; Carr, Jonathan J; Bardien, Soraya S
Publication Date: 2021

Variant appearance in text: NAT8: 428T>C; F143S; rs13538
PubMed Link: 33770142
Variant Present in the following documents:
  • pone.0249324.s003.xlsx, sheet 2
View BVdb publication page



NAT8 Variants, N-Acetylated Amino Acids, and Progression of CKD.

Clinical Journal Of The American Society Of Nephrology : Cjasn
Luo, Shengyuan S; Surapaneni, Aditya A; Zheng, Zihe Z; Rhee, Eugene P EP; Coresh, Josef J; Hung, Adriana M AM; Nadkarni, Girish N GN; Yu, Bing B; Boerwinkle, Eric E; Tin, Adrienne A; Arking, Dan E DE; Steinbrenner, Inga I; Schlosser, Pascal P; Köttgen, Anna A; Grams, Morgan E ME
Publication Date: 2020-12-31

Variant appearance in text: NAT8: Phe143Ser; rs13538
PubMed Link: 33380473
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic studies of urinary metabolites illuminate mechanisms of detoxification and excretion in humans.

Nature Genetics
Schlosser, Pascal P; Li, Yong Y; Sekula, Peggy P; Raffler, Johannes J; Grundner-Culemann, Franziska F; Pietzner, Maik M; Cheng, Yurong Y; Wuttke, Matthias M; Steinbrenner, Inga I; Schultheiss, Ulla T UT; Kotsis, Fruzsina F; Kacprowski, Tim T; Forer, Lukas L; Hausknecht, Birgit B; Ekici, Arif B AB; Nauck, Matthias M; Völker, Uwe U; , ; Walz, Gerd G; Oefner, Peter J PJ; Kronenberg, Florian F; Mohney, Robert P RP; Köttgen, Michael M; Suhre, Karsten K; Eckardt, Kai-Uwe KU; Kastenmüller, Gabi G; Köttgen, Anna A
Publication Date: 2020-02

Variant appearance in text: rs13538
PubMed Link: 31959995
Variant Present in the following documents:
  • Main text
View BVdb publication page



Extensive disruption of protein interactions by genetic variants across the allele frequency spectrum in human populations.

Nature Communications
Fragoza, Robert R; Das, Jishnu J; Wierbowski, Shayne D SD; Liang, Jin J; Tran, Tina N TN; Liang, Siqi S; Beltran, Juan F JF; Rivera-Erick, Christen A CA; Ye, Kaixiong K; Wang, Ting-Yi TY; Yao, Li L; Mort, Matthew M; Stenson, Peter D PD; Cooper, David N DN; Wei, Xiaomu X; Keinan, Alon A; Schimenti, John C JC; Clark, Andrew G AG; Yu, Haiyuan H
Publication Date: 2019-09-12

Variant appearance in text: NAT8: 428T>C; F143S; rs13538
PubMed Link: 31515488
Variant Present in the following documents:
  • 41467_2019_11959_MOESM6_ESM.xlsx, sheet 1
  • 41467_2019_11959_MOESM11_ESM.xlsx, sheet 1
View BVdb publication page



A reference collection of patient-derived cell line and xenograft models of proneural, classical and mesenchymal glioblastoma.

Scientific Reports
Stringer, Brett W BW; Day, Bryan W BW; D'Souza, Rochelle C J RCJ; Jamieson, Paul R PR; Ensbey, Kathleen S KS; Bruce, Zara C ZC; Lim, Yi Chieh YC; Goasdoué, Kate K; Offenhäuser, Carolin C; Akgül, Seçkin S; Allan, Suzanne S; Robertson, Thomas T; Lucas, Peter P; Tollesson, Gert G; Campbell, Scott S; Winter, Craig C; Do, Hongdo H; Dobrovic, Alexander A; Inglis, Po-Ling PL; Jeffree, Rosalind L RL; Johns, Terrance G TG; Boyd, Andrew W AW
Publication Date: 2019-03-20

Variant appearance in text: NAT8: F143S; rs13538
PubMed Link: 30894629
Variant Present in the following documents:
  • 41598_2019_41277_MOESM4_ESM.xlsx, sheet 9
  • 41598_2019_41277_MOESM4_ESM.xlsx, sheet 3
  • 41598_2019_41277_MOESM4_ESM.xlsx, sheet 10
  • 41598_2019_41277_MOESM4_ESM.xlsx, sheet 12
View BVdb publication page



Multiple genetic mutations caused by NKX6.3 depletion contribute to gastric tumorigenesis.

Scientific Reports
Yoon, Jung Hwan JH; Kim, Olga O; Eun, Jung Woo JW; Choi, Sung Sook SS; Ashktorab, Hassan H; Smoot, Duane T DT; Nam, Suk Woo SW; Park, Won Sang WS
Publication Date: 2018-12-04

Variant appearance in text: NAT8: F143S; rs13538
PubMed Link: 30514953
Variant Present in the following documents:
  • 41598_2018_35733_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Role of Alström syndrome 1 in the regulation of blood pressure and renal function.

Jci Insight
Jaykumar, Ankita Bachhawat AB; Caceres, Paulo S PS; King-Medina, Keyona N KN; Liao, Tang-Dong TD; Datta, Indrani I; Maskey, Dipak D; Naggert, Jürgen K JK; Mendez, Mariela M; Beierwaltes, William H WH; Ortiz, Pablo A PA
Publication Date: 2018-11-02

Variant appearance in text: rs13538
PubMed Link: 30385718
Variant Present in the following documents:
  • Main text
View BVdb publication page



Renal compartment-specific genetic variation analyses identify new pathways in chronic kidney disease.

Nature Medicine
Qiu, Chengxiang C; Huang, Shizheng S; Park, Jihwan J; Park, YoSon Y; Ko, Yi-An YA; Seasock, Matthew J MJ; Bryer, Joshua S JS; Xu, Xiang-Xi XX; Song, Wen-Chao WC; Palmer, Matthew M; Hill, Jon J; Guarnieri, Paolo P; Hawkins, Julie J; Boustany-Kari, Carine M CM; Pullen, Steven S SS; Brown, Christopher D CD; Susztak, Katalin K
Publication Date: 2018-11

Variant appearance in text: rs13538
PubMed Link: 30275566
Variant Present in the following documents:
  • Main text
View BVdb publication page



The role of genetic variation of human metabolism for BMI, mental traits and mental disorders.

Molecular Metabolism
Hebebrand, Johannes J; Peters, Triinu T; Schijven, Dick D; Hebebrand, Moritz M; Grasemann, Corinna C; Winkler, Thomas W TW; Heid, Iris M IM; Antel, Jochen J; Föcker, Manuel M; Tegeler, Lisa L; Brauner, Lena L; Adan, Roger A H RAH; Luykx, Jurjen J JJ; Correll, Christoph U CU; König, Inke R IR; Hinney, Anke A; Libuda, Lars L
Publication Date: 2018-06

Variant appearance in text: rs13538
PubMed Link: 29673576
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



Whole-exome sequencing identifies common and rare variant metabolic QTLs in a Middle Eastern population.

Nature Communications
Yousri, Noha A NA; Fakhro, Khalid A KA; Robay, Amal A; Rodriguez-Flores, Juan L JL; Mohney, Robert P RP; Zeriri, Hassina H; Odeh, Tala T; Kader, Sara Abdul SA; Aldous, Eman K EK; Thareja, Gaurav G; Kumar, Manish M; Al-Shakaki, Alya A; Chidiac, Omar M OM; Mohamoud, Yasmin A YA; Mezey, Jason G JG; Malek, Joel A JA; Crystal, Ronald G RG; Suhre, Karsten K
Publication Date: 2018-01-23

Variant appearance in text: NAT8: Phe143Ser; rs13538
PubMed Link: 29362361
Variant Present in the following documents:
  • Main text
  • 41467_2017_1972_MOESM8_ESM.xlsx, sheet 1
  • 41467_2017_1972_MOESM5_ESM.xlsx, sheet 1
  • 41467_2017_Article_1972.pdf
View BVdb publication page



Lessons from CKD-Related Genetic Association Studies-Moving Forward.

Clinical Journal Of The American Society Of Nephrology : Cjasn
Limou, Sophie S; Vince, Nicolas N; Parsa, Afshin A
Publication Date: 2018-01-06

Variant appearance in text: rs13538
PubMed Link: 29242368
Variant Present in the following documents:
  • Main text
View BVdb publication page



Chromatin Conformation Links Distal Target Genes to CKD Loci.

Journal Of The American Society Of Nephrology : Jasn
Brandt, Maarten M MM; Meddens, Claartje A CA; Louzao-Martinez, Laura L; van den Dungen, Noortje A M NAM; Lansu, Nico R NR; Nieuwenhuis, Edward E S EES; Duncker, Dirk J DJ; Verhaar, Marianne C MC; Joles, Jaap A JA; Mokry, Michal M; Cheng, Caroline C
Publication Date: 2018-02

Variant appearance in text: rs13538
PubMed Link: 29093029
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic-Variation-Driven Gene-Expression Changes Highlight Genes with Important Functions for Kidney Disease.

American Journal Of Human Genetics
Ko, Yi-An YA; Yi, Huiguang H; Qiu, Chengxiang C; Huang, Shizheng S; Park, Jihwan J; Ledo, Nora N; Köttgen, Anna A; Li, Hongzhe H; Rader, Daniel J DJ; Pack, Michael A MA; Brown, Christopher D CD; Susztak, Katalin K
Publication Date: 2017-06-01

Variant appearance in text: rs13538
PubMed Link: 28575649
Variant Present in the following documents:
  • Main text
View BVdb publication page



1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.

Scientific Reports
Gorski, Mathias M; van der Most, Peter J PJ; Teumer, Alexander A; Chu, Audrey Y AY; Li, Man M; Mijatovic, Vladan V; Nolte, Ilja M IM; Cocca, Massimiliano M; Taliun, Daniel D; Gomez, Felicia F; Li, Yong Y; Tayo, Bamidele B; Tin, Adrienne A; Feitosa, Mary F MF; Aspelund, Thor T; Attia, John J; Biffar, Reiner R; Bochud, Murielle M; Boerwinkle, Eric E; Borecki, Ingrid I; Bottinger, Erwin P EP; Chen, Ming-Huei MH; Chouraki, Vincent V; Ciullo, Marina M; Coresh, Josef J; Cornelis, Marilyn C MC; Curhan, Gary C GC; d'Adamo, Adamo Pio AP; Dehghan, Abbas A; Dengler, Laura L; Ding, Jingzhong J; Eiriksdottir, Gudny G; Endlich, Karlhans K; Enroth, Stefan S; Esko, Tõnu T; Franco, Oscar H OH; Gasparini, Paolo P; Gieger, Christian C; Girotto, Giorgia G; Gottesman, Omri O; Gudnason, Vilmundur V; Gyllensten, Ulf U; Hancock, Stephen J SJ; Harris, Tamara B TB; Helmer, Catherine C; Höllerer, Simon S; Hofer, Edith E; Hofman, Albert A; Holliday, Elizabeth G EG; Homuth, Georg G; Hu, Frank B FB; Huth, Cornelia C; Hutri-Kähönen, Nina N; Hwang, Shih-Jen SJ; Imboden, Medea M; Johansson, Åsa Å; Kähönen, Mika M; König, Wolfgang W; Kramer, Holly H; Krämer, Bernhard K BK; Kumar, Ashish A; Kutalik, Zoltan Z; Lambert, Jean-Charles JC; Launer, Lenore J LJ; Lehtimäki, Terho T; de Borst, Martin M; Navis, Gerjan G; Swertz, Morris M; Liu, Yongmei Y; Lohman, Kurt K; Loos, Ruth J F RJF; Lu, Yingchang Y; Lyytikäinen, Leo-Pekka LP; McEvoy, Mark A MA; Meisinger, Christa C; Meitinger, Thomas T; Metspalu, Andres A; Metzger, Marie M; Mihailov, Evelin E; Mitchell, Paul P; Nauck, Matthias M; Oldehinkel, Albertine J AJ; Olden, Matthias M; Wjh Penninx, Brenda B; Pistis, Giorgio G; Pramstaller, Peter P PP; Probst-Hensch, Nicole N; Raitakari, Olli T OT; Rettig, Rainer R; Ridker, Paul M PM; Rivadeneira, Fernando F; Robino, Antonietta A; Rosas, Sylvia E SE; Ruderfer, Douglas D; Ruggiero, Daniela D; Saba, Yasaman Y; Sala, Cinzia C; Schmidt, Helena H; Schmidt, Reinhold R; Scott, Rodney J RJ; Sedaghat, Sanaz S; Smith, Albert V AV; Sorice, Rossella R; Stengel, Benedicte B; Stracke, Sylvia S; Strauch, Konstantin K; Toniolo, Daniela D; Uitterlinden, Andre G AG; Ulivi, Sheila S; Viikari, Jorma S JS; Völker, Uwe U; Vollenweider, Peter P; Völzke, Henry H; Vuckovic, Dragana D; Waldenberger, Melanie M; Jin Wang, Jie J; Yang, Qiong Q; Chasman, Daniel I DI; Tromp, Gerard G; Snieder, Harold H; Heid, Iris M IM; Fox, Caroline S CS; Köttgen, Anna A; Pattaro, Cristian C; Böger, Carsten A CA; Fuchsberger, Christian C
Publication Date: 2017-04-28

Variant appearance in text: rs13538
PubMed Link: 28452372
Variant Present in the following documents:
  • srep45040-s1.pdf
View BVdb publication page



Genetic epidemiology in kidney disease.

Nephrology, Dialysis, Transplantation : Official Publication Of The European Dialysis And Transplant Association - European Renal Association
Ainsworth, Hannah C HC; Langefeld, Carl D CD; Freedman, Barry I BI
Publication Date: 2017-04-01

Variant appearance in text: rs13538
PubMed Link: 28201750
Variant Present in the following documents:
  • Main text
View BVdb publication page



Whole genome sequence analysis of serum amino acid levels.

Genome Biology
Yu, Bing B; de Vries, Paul S PS; Metcalf, Ginger A GA; Wang, Zhe Z; Feofanova, Elena V EV; Liu, Xiaoming X; Muzny, Donna Marie DM; Wagenknecht, Lynne E LE; Gibbs, Richard A RA; Morrison, Alanna C AC; Boerwinkle, Eric E
Publication Date: 2016-11-24

Variant appearance in text: rs13538
PubMed Link: 27884205
Variant Present in the following documents:
  • Main text
  • 13059_2016_Article_1106.pdf
View BVdb publication page



Clonal relationships between lobular carcinoma in situ and other breast malignancies.

Breast Cancer Research : Bcr
Begg, Colin B CB; Ostrovnaya, Irina I; Carniello, Jose V Scarpa JV; Sakr, Rita A RA; Giri, Dilip D; Towers, Russell R; Schizas, Michail M; De Brot, Marina M; Andrade, Victor P VP; Mauguen, Audrey A; Seshan, Venkatraman E VE; King, Tari A TA
Publication Date: 2016-06-23

Variant appearance in text: NAT8: F143S
PubMed Link: 27334989
Variant Present in the following documents:
  • 13058_2016_727_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



PredictSNP2: A Unified Platform for Accurately Evaluating SNP Effects by Exploiting the Different Characteristics of Variants in Distinct Genomic Regions.

Plos Computational Biology
Bendl, Jaroslav J; Musil, Miloš M; Štourač, Jan J; Zendulka, Jaroslav J; Damborský, Jiří J; Brezovský, Jan J
Publication Date: 2016-05

Variant appearance in text: NAT8: F143S
PubMed Link: 27224906
Variant Present in the following documents:
  • pcbi.1004962.s005.xlsx, sheet 3
View BVdb publication page



Influence of common genetic variants on childhood kidney outcomes.

Pediatric Research
Miliku, Kozeta K; Vogelezang, Suzanne S; Franco, Oscar H OH; Hofman, Albert A; Jaddoe, Vincent W V VW; Felix, Janine F JF
Publication Date: 2016-07

Variant appearance in text: rs13538
PubMed Link: 26959481
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.

Nature Communications
Pattaro, Cristian C; Teumer, Alexander A; Gorski, Mathias M; Chu, Audrey Y AY; Li, Man M; Mijatovic, Vladan V; Garnaas, Maija M; Tin, Adrienne A; Sorice, Rossella R; Li, Yong Y; Taliun, Daniel D; Olden, Matthias M; Foster, Meredith M; Yang, Qiong Q; Chen, Ming-Huei MH; Pers, Tune H TH; Johnson, Andrew D AD; Ko, Yi-An YA; Fuchsberger, Christian C; Tayo, Bamidele B; Nalls, Michael M; Feitosa, Mary F MF; Isaacs, Aaron A; Dehghan, Abbas A; d'Adamo, Pio P; Adeyemo, Adebowale A; Dieffenbach, Aida Karina AK; Zonderman, Alan B AB; Nolte, Ilja M IM; van der Most, Peter J PJ; Wright, Alan F AF; Shuldiner, Alan R AR; Morrison, Alanna C AC; Hofman, Albert A; Smith, Albert V AV; Dreisbach, Albert W AW; Franke, Andre A; Uitterlinden, Andre G AG; Metspalu, Andres A; Tonjes, Anke A; Lupo, Antonio A; Robino, Antonietta A; Johansson, Åsa Å; Demirkan, Ayse A; Kollerits, Barbara B; Freedman, Barry I BI; Ponte, Belen B; Oostra, Ben A BA; Paulweber, Bernhard B; Krämer, Bernhard K BK; Mitchell, Braxton D BD; Buckley, Brendan M BM; Peralta, Carmen A CA; Hayward, Caroline C; Helmer, Catherine C; Rotimi, Charles N CN; Shaffer, Christian M CM; Müller, Christian C; Sala, Cinzia C; van Duijn, Cornelia M CM; Saint-Pierre, Aude A; Ackermann, Daniel D; Shriner, Daniel D; Ruggiero, Daniela D; Toniolo, Daniela D; Lu, Yingchang Y; Cusi, Daniele D; Czamara, Darina D; Ellinghaus, David D; Siscovick, David S DS; Ruderfer, Douglas D; Gieger, Christian C; Grallert, Harald H; Rochtchina, Elena E; Atkinson, Elizabeth J EJ; Holliday, Elizabeth G EG; Boerwinkle, Eric E; Salvi, Erika E; Bottinger, Erwin P EP; Murgia, Federico F; Rivadeneira, Fernando F; Ernst, Florian F; Kronenberg, Florian F; Hu, Frank B FB; Navis, Gerjan J GJ; Curhan, Gary C GC; Ehret, George B GB; Homuth, Georg G; Coassin, Stefan S; Thun, Gian-Andri GA; Pistis, Giorgio G; Gambaro, Giovanni G; Malerba, Giovanni G; Montgomery, Grant W GW; Eiriksdottir, Gudny G; Jacobs, Gunnar G; Li, Guo G; Wichmann, H-Erich HE; Campbell, Harry H; Schmidt, Helena H; Wallaschofski, Henri H; Völzke, Henry H; Brenner, Hermann H; Kroemer, Heyo K HK; Kramer, Holly H; Lin, Honghuang H; Leach, I Mateo IM; Ford, Ian I; Guessous, Idris I; Rudan, Igor I; Prokopenko, Inga I; Borecki, Ingrid I; Heid, Iris M IM; Kolcic, Ivana I; Persico, Ivana I; Jukema, J Wouter JW; Wilson, James F JF; Felix, Janine F JF; Divers, Jasmin J; Lambert, Jean-Charles JC; Stafford, Jeanette M JM; Gaspoz, Jean-Michel JM; Smith, Jennifer A JA; Faul, Jessica D JD; Wang, Jie Jin JJ; Ding, Jingzhong J; Hirschhorn, Joel N JN; Attia, John J; Whitfield, John B JB; Chalmers, John J; Viikari, Jorma J; Coresh, Josef J; Denny, Joshua C JC; Karjalainen, Juha J; Fernandes, Jyotika K JK; Endlich, Karlhans K; Butterbach, Katja K; Keene, Keith L KL; Lohman, Kurt K; Portas, Laura L; Launer, Lenore J LJ; Lyytikäinen, Leo-Pekka LP; Yengo, Loic L; Franke, Lude L; Ferrucci, Luigi L; Rose, Lynda M LM; Kedenko, Lyudmyla L; Rao, Madhumathi M; Struchalin, Maksim M; Kleber, Marcus E ME; Cavalieri, Margherita M; Haun, Margot M; Cornelis, Marilyn C MC; Ciullo, Marina M; Pirastu, Mario M; de Andrade, Mariza M; McEvoy, Mark A MA; Woodward, Mark M; Adam, Martin M; Cocca, Massimiliano M; Nauck, Matthias M; Imboden, Medea M; Waldenberger, Melanie M; Pruijm, Menno M; Metzger, Marie M; Stumvoll, Michael M; Evans, Michele K MK; Sale, Michele M MM; Kähönen, Mika M; Boban, Mladen M; Bochud, Murielle M; Rheinberger, Myriam M; Verweij, Niek N; Bouatia-Naji, Nabila N; Martin, Nicholas G NG; Hastie, Nick N; Probst-Hensch, Nicole N; Soranzo, Nicole N; Devuyst, Olivier O; Raitakari, Olli O; Gottesman, Omri O; Franco, Oscar H OH; Polasek, Ozren O; Gasparini, Paolo P; Munroe, Patricia B PB; Ridker, Paul M PM; Mitchell, Paul P; Muntner, Paul P; Meisinger, Christa C; Smit, Johannes H JH; , ; , ; , ; , ; , ; Kovacs, Peter P; Wild, Philipp S PS; Froguel, Philippe P; Rettig, Rainer R; Mägi, Reedik R; Biffar, Reiner R; Schmidt, Reinhold R; Middelberg, Rita P S RP; Carroll, Robert J RJ; Penninx, Brenda W BW; Scott, Rodney J RJ; Katz, Ronit R; Sedaghat, Sanaz S; Wild, Sarah H SH; Kardia, Sharon L R SL; Ulivi, Sheila S; Hwang, Shih-Jen SJ; Enroth, Stefan S; Kloiber, Stefan S; Trompet, Stella S; Stengel, Benedicte B; Hancock, Stephen J SJ; Turner, Stephen T ST; Rosas, Sylvia E SE; Stracke, Sylvia S; Harris, Tamara B TB; Zeller, Tanja T; Zemunik, Tatijana T; Lehtimäki, Terho T; Illig, Thomas T; Aspelund, Thor T; Nikopensius, Tiit T; Esko, Tonu T; Tanaka, Toshiko T; Gyllensten, Ulf U; Völker, Uwe U; Emilsson, Valur V; Vitart, Veronique V; Aalto, Ville V; Gudnason, Vilmundur V; Chouraki, Vincent V; Chen, Wei-Min WM; Igl, Wilmar W; März, Winfried W; Koenig, Wolfgang W; Lieb, Wolfgang W; Loos, Ruth J F RJ; Liu, Yongmei Y; Snieder, Harold H; Pramstaller, Peter P PP; Parsa, Afshin A; O'Connell, Jeffrey R JR; Susztak, Katalin K; Hamet, Pavel P; Tremblay, Johanne J; de Boer, Ian H IH; Böger, Carsten A CA; Goessling, Wolfram W; Chasman, Daniel I DI; Köttgen, Anna A; Kao, W H Linda WH; Fox, Caroline S CS
Publication Date: 2016-01-21

Variant appearance in text: rs13538
PubMed Link: 26831199
Variant Present in the following documents:
  • ncomms10023-s1.pdf
  • ncomms10023.pdf
View BVdb publication page



Generation of a High Number of Healthy Erythroid Cells from Gene-Edited Pyruvate Kinase Deficiency Patient-Specific Induced Pluripotent Stem Cells.

Stem Cell Reports
Garate, Zita Z; Quintana-Bustamante, Oscar O; Crane, Ana M AM; Olivier, Emmanuel E; Poirot, Laurent L; Galetto, Roman R; Kosinski, Penelope P; Hill, Collin C; Kung, Charles C; Agirre, Xabi X; Orman, Israel I; Cerrato, Laura L; Alberquilla, Omaira O; Rodriguez-Fornes, Fatima F; Fusaki, Noemi N; Garcia-Sanchez, Felix F; Maia, Tabita M TM; Ribeiro, Maria L ML; Sevilla, Julian J; Prosper, Felipe F; Jin, Shengfang S; Mountford, Joanne J; Guenechea, Guillermo G; Gouble, Agnes A; Bueren, Juan A JA; Davis, Brian R BR; Segovia, Jose C JC
Publication Date: 2015-12-08

Variant appearance in text: NAT8: F143S; rs13538
PubMed Link: 26549847
Variant Present in the following documents:
  • mmc3.xlsx, sheet 2
  • mmc3.xlsx, sheet 1
  • mmc3.xlsx, sheet 3
View BVdb publication page



GESPA: classifying nsSNPs to predict disease association.

Bmc Bioinformatics
Khurana, Jay K JK; Reeder, Jay E JE; Shrimpton, Antony E AE; Thakar, Juilee J
Publication Date: 2015-07-25

Variant appearance in text: NAT8: F143S
PubMed Link: 26206375
Variant Present in the following documents:
  • 12859_2015_673_MOESM1_ESM.xls, sheet 4
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Dissecting the genetics of the human transcriptome identifies novel trait-related trans-eQTLs and corroborates the regulatory relevance of non-protein coding loci†.

Human Molecular Genetics
Kirsten, Holger H; Al-Hasani, Hoor H; Holdt, Lesca L; Gross, Arnd A; Beutner, Frank F; Krohn, Knut K; Horn, Katrin K; Ahnert, Peter P; Burkhardt, Ralph R; Reiche, Kristin K; Hackermüller, Jörg J; Löffler, Markus M; Teupser, Daniel D; Thiery, Joachim J; Scholz, Markus M
Publication Date: 2015-08-15

Variant appearance in text: rs13538
PubMed Link: 26019233
Variant Present in the following documents:
  • Main text
  • ddv194.pdf
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Proteogenomic analysis reveals exosomes are more oncogenic than ectosomes.

Oncotarget
Keerthikumar, Shivakumar S; Gangoda, Lahiru L; Liem, Michael M; Fonseka, Pamali P; Atukorala, Ishara I; Ozcitti, Cemil C; Mechler, Adam A; Adda, Christopher G CG; Ang, Ching-Seng CS; Mathivanan, Suresh S
Publication Date: 2015-06-20

Variant appearance in text: NAT8: F143S; rs13538
PubMed Link: 25944692
Variant Present in the following documents:
  • oncotarget-06-15375-s005.xlsx, sheet 2
View BVdb publication page



Whole genome sequencing of an ethnic Pathan (Pakhtun) from the north-west of Pakistan.

Bmc Genomics
Ilyas, Muhammad M; Kim, Jong-Soo JS; Cooper, Jesse J; Shin, Young-Ah YA; Kim, Hak-Min HM; Cho, Yun Sung YS; Hwang, Seungwoo S; Kim, Hyunho H; Moon, Jaewoo J; Chung, Oksung O; Jun, JeHoon J; Rastogi, Achal A; Song, Sanghoon S; Ko, Junsu J; Manica, Andrea A; Rahman, Ziaur Z; Husnain, Tayyab T; Bhak, Jong J
Publication Date: 2015-03-12

Variant appearance in text: NAT8: F143S; rs13538
PubMed Link: 25887915
Variant Present in the following documents:
  • 12864_2015_1290_MOESM7_ESM.xlsx, sheet 1
View BVdb publication page



Whole-exome sequencing of pancreatic cancer defines genetic diversity and therapeutic targets.

Nature Communications
Witkiewicz, Agnieszka K AK; McMillan, Elizabeth A EA; Balaji, Uthra U; Baek, GuemHee G; Lin, Wan-Chi WC; Mansour, John J; Mollaee, Mehri M; Wagner, Kay-Uwe KU; Koduru, Prasad P; Yopp, Adam A; Choti, Michael A MA; Yeo, Charles J CJ; McCue, Peter P; White, Michael A MA; Knudsen, Erik S ES
Publication Date: 2015-04-09

Variant appearance in text: NAT8: F143S; rs13538
PubMed Link: 25855536
Variant Present in the following documents:
  • ncomms7744-s2.xlsx, sheet 1
View BVdb publication page



Whole-genome sequencing of the world's oldest people.

Plos One
Gierman, Hinco J HJ; Fortney, Kristen K; Roach, Jared C JC; Coles, Natalie S NS; Li, Hong H; Glusman, Gustavo G; Markov, Glenn J GJ; Smith, Justin D JD; Hood, Leroy L; Coles, L Stephen LS; Kim, Stuart K SK
Publication Date: 2014

Variant appearance in text: NAT8: F143S; rs13538
PubMed Link: 25390934
Variant Present in the following documents:
  • pone.0112430.s004.xlsx, sheet 1
View BVdb publication page



A gene variant in CERS2 is associated with rate of increase in albuminuria in patients with diabetes from ONTARGET and TRANSCEND.

Plos One
Shiffman, Dov D; Pare, Guillaume G; Oberbauer, Rainer R; Louie, Judy Z JZ; Rowland, Charles M CM; Devlin, James J JJ; Mann, Johannes F JF; McQueen, Matthew J MJ
Publication Date: 2014

Variant appearance in text: rs13538
PubMed Link: 25238615
Variant Present in the following documents:
  • Main text
View BVdb publication page



Integrative biology identifies shared transcriptional networks in CKD.

Journal Of The American Society Of Nephrology : Jasn
Martini, Sebastian S; Nair, Viji V; Keller, Benjamin J BJ; Eichinger, Felix F; Hawkins, Jennifer J JJ; Randolph, Ann A; Böger, Carsten A CA; Gadegbeku, Crystal A CA; Fox, Caroline S CS; Cohen, Clemens D CD; Kretzler, Matthias M; , ; , ; ,
Publication Date: 2014-11

Variant appearance in text: rs13538
PubMed Link: 24925724
Variant Present in the following documents:
  • Main text
View BVdb publication page



VarMod: modelling the functional effects of non-synonymous variants.

Nucleic Acids Research
Pappalardo, Morena M; Wass, Mark N MN
Publication Date: 2014-07

Variant appearance in text: rs13538
PubMed Link: 24906884
Variant Present in the following documents:
  • Main text
  • gku483.pdf
View BVdb publication page



Genetic determinants influencing human serum metabolome among African Americans.

Plos Genetics
Yu, Bing B; Zheng, Yan Y; Alexander, Danny D; Morrison, Alanna C AC; Coresh, Josef J; Boerwinkle, Eric E
Publication Date: 2014-03

Variant appearance in text: rs13538
PubMed Link: 24625756
Variant Present in the following documents:
  • Main text
  • pgen.1004212.pdf
View BVdb publication page



Prevalence of CKD and its relationship to eGFR-related genetic loci and clinical risk factors in the SardiNIA study cohort.

Journal Of The American Society Of Nephrology : Jasn
Pani, Antonello A; Bragg-Gresham, Jennifer J; Masala, Marco M; Piras, Doloretta D; Atzeni, Alice A; Pilia, Maria G MG; Ferreli, Liana L; Balaci, Lenuta L; Curreli, Nicolò N; Delitala, Alessandro A; Loi, Francesco F; Abecasis, Gonçalo R GR; Schlessinger, David D; Cucca, Francesco F
Publication Date: 2014-07

Variant appearance in text: rs13538
PubMed Link: 24511125
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association study of a heart failure related metabolomic profile among African Americans in the Atherosclerosis Risk in Communities (ARIC) study.

Genetic Epidemiology
Yu, Bing B; Zheng, Yan Y; Alexander, Danny D; Manolio, Teri A TA; Alonso, Alvaro A; Nettleton, Jennifer A JA; Boerwinkle, Eric E
Publication Date: 2013-12

Variant appearance in text: NAT8: F143S; rs13538
PubMed Link: 23934736
Variant Present in the following documents:
  • Main text
View BVdb publication page



Assessment of computational methods for predicting the effects of missense mutations in human cancers.

Bmc Genomics
Gnad, Florian F; Baucom, Albion A; Mukhyala, Kiran K; Manning, Gerard G; Zhang, Zemin Z
Publication Date: 2013

Variant appearance in text: rs13538
PubMed Link: 23819521
Variant Present in the following documents:
  • 1471-2164-14-S3-S7-S1.xlsx, sheet 2
View BVdb publication page



Investigation of known estimated glomerular filtration rate loci in patients with type 2 diabetes.

Diabetic Medicine : A Journal Of The British Diabetic Association
Deshmukh, H A HA; Palmer, C N A CN; Morris, A D AD; Colhoun, H M HM
Publication Date: 2013-10

Variant appearance in text: rs13538
PubMed Link: 23586973
Variant Present in the following documents:
  • Main text
View BVdb publication page



Overlap between common genetic polymorphisms underpinning kidney traits and cardiovascular disease phenotypes: the CKDGen consortium.

American Journal Of Kidney Diseases : The Official Journal Of The National Kidney Foundation
Olden, Matthias M; Teumer, Alexander A; Bochud, Murielle M; Pattaro, Cristian C; Köttgen, Anna A; Turner, Stephen T ST; Rettig, Rainer R; Chen, Ming-Huei MH; Dehghan, Abbas A; Bastardot, Francois F; Schmidt, Reinhold R; Vollenweider, Peter P; Schunkert, Heribert H; Reilly, Muredach P MP; Fornage, Myriam M; Launer, Lenore J LJ; Verwoert, Germaine C GC; Mitchell, Gary F GF; Bis, Joshua C JC; O'Donnell, Christopher J CJ; Cheng, Ching-Yu CY; Sim, Xueling X; Siscovick, David S DS; Coresh, Josef J; Kao, W H Linda WH; Fox, Caroline S CS; O'Seaghdha, Conall M CM; ,
Publication Date: 2013-06

Variant appearance in text: rs13538
PubMed Link: 23474010
Variant Present in the following documents:
  • Main text
View BVdb publication page



Multiple loci associated with renal function in African Americans.

Plos One
Shriner, Daniel D; Herbert, Alan A; Doumatey, Ayo P AP; Zhou, Jie J; Huang, Hanxia H; Erdos, Michael R MR; Chen, Guanjie G; Gerry, Norman P NP; Christman, Michael F MF; Adeyemo, Adebowale A; Rotimi, Charles N CN
Publication Date: 2012

Variant appearance in text: rs13538
PubMed Link: 23028791
Variant Present in the following documents:
  • Main text
  • pone.0045112.pdf
View BVdb publication page



Genetic architecture of microRNA expression: implications for the transcriptome and complex traits.

American Journal Of Human Genetics
Gamazon, Eric R ER; Ziliak, Dana D; Im, Hae Kyung HK; LaCroix, Bonnie B; Park, Danny S DS; Cox, Nancy J NJ; Huang, R Stephanie RS
Publication Date: 2012-06-08

Variant appearance in text: rs13538
PubMed Link: 22658545
Variant Present in the following documents:
  • Main text
View BVdb publication page



Validated SNPs for eGFR and their associations with albuminuria.

Human Molecular Genetics
Ellis, Jaclyn W JW; Chen, Ming-Huei MH; Foster, Meredith C MC; Liu, Ching-Ti CT; Larson, Martin G MG; de Boer, Ian I; Köttgen, Anna A; Parsa, Afshin A; Bochud, Murielle M; Böger, Carsten A CA; Kao, Linda L; Fox, Caroline S CS; O'Seaghdha, Conall M CM; , ; ,
Publication Date: 2012-07-15

Variant appearance in text: rs13538
PubMed Link: 22492995
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association studies of chronic kidney disease: what have we learned?

Nature Reviews. Nephrology
O'Seaghdha, Conall M CM; Fox, Caroline S CS
Publication Date: 2011-12-06

Variant appearance in text: rs13538
PubMed Link: 22143329
Variant Present in the following documents:
  • Main text
View BVdb publication page



Alström syndrome: genetics and clinical overview.

Current Genomics
Marshall, Jan D JD; Maffei, Pietro P; Collin, Gayle B GB; Naggert, Jürgen K JK
Publication Date: 2011-05

Variant appearance in text: rs13538
PubMed Link: 22043170
Variant Present in the following documents:
  • Main text
  • CG-12-225.pdf
View BVdb publication page



Association of eGFR-Related Loci Identified by GWAS with Incident CKD and ESRD.

Plos Genetics
Böger, Carsten A CA; Gorski, Mathias M; Li, Man M; Hoffmann, Michael M MM; Huang, Chunmei C; Yang, Qiong Q; Teumer, Alexander A; Krane, Vera V; O'Seaghdha, Conall M CM; Kutalik, Zoltán Z; Wichmann, H-Erich HE; Haak, Thomas T; Boes, Eva E; Coassin, Stefan S; Coresh, Josef J; Kollerits, Barbara B; Haun, Margot M; Paulweber, Bernhard B; Köttgen, Anna A; Li, Guo G; Shlipak, Michael G MG; Powe, Neil N; Hwang, Shih-Jen SJ; Dehghan, Abbas A; Rivadeneira, Fernando F; Uitterlinden, André A; Hofman, Albert A; Beckmann, Jacques S JS; Krämer, Bernhard K BK; Witteman, Jacqueline J; Bochud, Murielle M; Siscovick, David D; Rettig, Rainer R; Kronenberg, Florian F; Wanner, Christoph C; Thadhani, Ravi I RI; Heid, Iris M IM; Fox, Caroline S CS; Kao, W H WH; ,
Publication Date: 2011-09

Variant appearance in text: rs13538
PubMed Link: 21980298
Variant Present in the following documents:
  • Main text
View BVdb publication page



A genome-wide metabolic QTL analysis in Europeans implicates two loci shaped by recent positive selection.

Plos Genetics
Nicholson, George G; Rantalainen, Mattias M; Li, Jia V JV; Maher, Anthony D AD; Malmodin, Daniel D; Ahmadi, Kourosh R KR; Faber, Johan H JH; Barrett, Amy A; Min, Josine L JL; Rayner, N William NW; Toft, Henrik H; Krestyaninova, Maria M; Viksna, Juris J; Neogi, Sudeshna Guha SG; Dumas, Marc-Emmanuel ME; Sarkans, Ugis U; , ; Donnelly, Peter P; Illig, Thomas T; Adamski, Jerzy J; Suhre, Karsten K; Allen, Maxine M; Zondervan, Krina T KT; Spector, Tim D TD; Nicholson, Jeremy K JK; Lindon, John C JC; Baunsgaard, Dorrit D; Holmes, Elaine E; McCarthy, Mark I MI; Holmes, Chris C CC
Publication Date: 2011-09

Variant appearance in text: rs13538
PubMed Link: 21931564
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic association for renal traits among participants of African ancestry reveals new loci for renal function.

Plos Genetics
Liu, Ching-Ti CT; Garnaas, Maija K MK; Tin, Adrienne A; Kottgen, Anna A; Franceschini, Nora N; Peralta, Carmen A CA; de Boer, Ian H IH; Lu, Xiaoning X; Atkinson, Elizabeth E; Ding, Jingzhong J; Nalls, Michael M; Shriner, Daniel D; Coresh, Josef J; Kutlar, Abdullah A; Bibbins-Domingo, Kirsten K; Siscovick, David D; Akylbekova, Ermeg E; Wyatt, Sharon S; Astor, Brad B; Mychaleckjy, Josef J; Li, Man M; Reilly, Muredach P MP; Townsend, Raymond R RR; Adeyemo, Adebowale A; Zonderman, Alan B AB; de Andrade, Mariza M; Turner, Stephen T ST; Mosley, Thomas H TH; Harris, Tamara B TB; , ; Rotimi, Charles N CN; Liu, Yongmei Y; Kardia, Sharon L R SL; Evans, Michele K MK; Shlipak, Michael G MG; Kramer, Holly H; Flessner, Michael F MF; Dreisbach, Albert W AW; Goessling, Wolfram W; Cupples, L Adrienne LA; Kao, W Linda WL; Fox, Caroline S CS
Publication Date: 2011-09

Variant appearance in text: rs13538
PubMed Link: 21931561
Variant Present in the following documents:
  • Main text
View BVdb publication page



Molecular identification of NAT8 as the enzyme that acetylates cysteine S-conjugates to mercapturic acids.

The Journal Of Biological Chemistry
Veiga-da-Cunha, Maria M; Tyteca, Donatienne D; Stroobant, Vincent V; Courtoy, Pierre J PJ; Opperdoes, Fred R FR; Van Schaftingen, Emile E
Publication Date: 2010-06-11

Variant appearance in text: NAT8: F143S
PubMed Link: 20392701
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic loci influencing kidney function and chronic kidney disease.

Nature Genetics
Chambers, John C JC; Zhang, Weihua W; Lord, Graham M GM; van der Harst, Pim P; Lawlor, Debbie A DA; Sehmi, Joban S JS; Gale, Daniel P DP; Wass, Mark N MN; Ahmadi, Kourosh R KR; Bakker, Stephan J L SJ; Beckmann, Jacqui J; Bilo, Henk J G HJ; Bochud, Murielle M; Brown, Morris J MJ; Caulfield, Mark J MJ; Connell, John M C JM; Cook, H Terence HT; Cotlarciuc, Ioana I; Davey Smith, George G; de Silva, Ranil R; Deng, Guohong G; Devuyst, Olivier O; Dikkeschei, Lambert D LD; Dimkovic, Nada N; Dockrell, Mark M; Dominiczak, Anna A; Ebrahim, Shah S; Eggermann, Thomas T; Farrall, Martin M; Ferrucci, Luigi L; Floege, Jurgen J; Forouhi, Nita G NG; Gansevoort, Ron T RT; Han, Xijin X; Hedblad, Bo B; Homan van der Heide, Jaap J JJ; Hepkema, Bouke G BG; Hernandez-Fuentes, Maria M; Hypponen, Elina E; Johnson, Toby T; de Jong, Paul E PE; Kleefstra, Nanne N; Lagou, Vasiliki V; Lapsley, Marta M; Li, Yun Y; Loos, Ruth J F RJ; Luan, Jian'an J; Luttropp, Karin K; Maréchal, Céline C; Melander, Olle O; Munroe, Patricia B PB; Nordfors, Louise L; Parsa, Afshin A; Peltonen, Leena L; Penninx, Brenda W BW; Perucha, Esperanza E; Pouta, Anneli A; Prokopenko, Inga I; Roderick, Paul J PJ; Ruokonen, Aimo A; Samani, Nilesh J NJ; Sanna, Serena S; Schalling, Martin M; Schlessinger, David D; Schlieper, Georg G; Seelen, Marc A J MA; Shuldiner, Alan R AR; Sjögren, Marketa M; Smit, Johannes H JH; Snieder, Harold H; Soranzo, Nicole N; Spector, Timothy D TD; Stenvinkel, Peter P; Sternberg, Michael J E MJ; Swaminathan, Ramasamyiyer R; Tanaka, Toshiko T; Ubink-Veltmaat, Lielith J LJ; Uda, Manuela M; Vollenweider, Peter P; Wallace, Chris C; Waterworth, Dawn D; Zerres, Klaus K; Waeber, Gerard G; Wareham, Nicholas J NJ; Maxwell, Patrick H PH; McCarthy, Mark I MI; Jarvelin, Marjo-Riitta MR; Mooser, Vincent V; Abecasis, Goncalo R GR; Lightstone, Liz L; Scott, James J; Navis, Gerjan G; Elliott, Paul P; Kooner, Jaspal S JS
Publication Date: 2010-05

Variant appearance in text: NAT8: F143S
PubMed Link: 20383145
Variant Present in the following documents:
  • Main text
View BVdb publication page



N-acetyltransferase 8, a positional candidate for blood pressure and renal regulation: resequencing, association and in silico study.

Bmc Medical Genetics
Juhanson, Peeter P; Kepp, Katrin K; Org, Elin E; Veldre, Gudrun G; Kelgo, Piret P; Rosenberg, Mai M; Viigimaa, Margus M; Laan, Maris M
Publication Date: 2008-04-10

Variant appearance in text: rs13538
PubMed Link: 18402670
Variant Present in the following documents:
  • Main text
  • 1471-2350-9-25.pdf
View BVdb publication page