CAT c.-20T>C

Variant ID: 11-34460541-T-C

NM_001752.3(CAT):c.-20T>C

This variant was identified in 37 publications

View GRCh38 version.




Publications:


Comprehensive proteogenomic characterization of early duodenal cancer reveals the carcinogenesis tracks of different subtypes.

Nature Communications
Li, Lingling L; Jiang, Dongxian D; Liu, Hui H; Guo, Chunmei C; Zhao, Rui R; Zhang, Qiao Q; Xu, Chen C; Qin, Zhaoyu Z; Feng, Jinwen J; Liu, Yang Y; Wang, Haixing H; Chen, Weijie W; Zhang, Xue X; Li, Bin B; Bai, Lin L; Tian, Sha S; Tan, Subei S; Yu, Zixiang Z; Chen, Lingli L; Huang, Jie J; Zhao, Jian-Yuan JY; Hou, Yingyong Y; Ding, Chen C
Publication Date: 2023-03-29

Variant appearance in text: rs1049982
PubMed Link: 36991000
Variant Present in the following documents:
  • 41467_2023_37221_MOESM5_ESM.xlsx, sheet 3
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: rs1049982
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Beneficial effects of mifepristone treatment in breast cancer patients selected by the progesterone receptor isoform ratio: Results from the MIPRA trial.

Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research
Elía, Andrés A; Saldain, Leo L; Vanzulli, Silvia I SI; Helguero, Luisa A LA; Lamb, Caroline A CA; Fabris, Victoria V; Pataccini, Gabriela G; Martínez-Vazquez, Paula P; Burruchaga, Javier J; Caillet-Bois, Ines I; Spengler, Eunice E; Acosta Haab, Gabriela G; Liguori, Marcos M; Castets, Alejandra A; Lovisi, Silvia S; Abascal, María F MF; Novaro, Virginia V; Sánchez, Jana J; Muñoz, Javier J; Belizán, Jose M JM; Abba, Martín C MC; Gass, Hugo H; Rojas, Paola P; Lanari, Claudia C
Publication Date: 2022-10-21

Variant appearance in text: rs1049982
PubMed Link: 36269797
Variant Present in the following documents:
  • ccr-22-2060_supplementary_table_s5_suppts5.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: rs1049982
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM15_ESM.xlsx, sheet 2
View BVdb publication page



A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts.

Human Genome Variation
Irum, Bushra B; Kabir, Firoz F; Shoshany, Nadav N; Khan, Shahid Y SY; Rauf, Bushra B; Naeem, Muhammad Asif MA; Qaiser, Tanveer A TA; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-09-08

Variant appearance in text: rs1049982
PubMed Link: 36075891
Variant Present in the following documents:
  • 41439_2022_208_MOESM4_ESM.xlsx, sheet 2
  • 41439_2022_208_MOESM3_ESM.xlsx, sheet 2
  • 41439_2022_208_MOESM5_ESM.xlsx, sheet 2
View BVdb publication page



Genetic Variations on Redox Control in Cardiometabolic Diseases: The Role of Nrf2.

Antioxidants (Basel, Switzerland)
Zazueta, Cecilia C; Jimenez-Uribe, Alexis Paulina AP; Pedraza-Chaverri, José J; Buelna-Chontal, Mabel M
Publication Date: 2022-03-06

Variant appearance in text: rs1049982
PubMed Link: 35326157
Variant Present in the following documents:
  • antioxidants-11-00507.pdf
View BVdb publication page



A novel missense variant in CEACAM16 gene causes autosomal dominant nonsyndromic hearing loss.

Annals Of Human Genetics
Zhang, Dejun D; Wu, Jie J; Yuan, Yongyi Y; Li, Xiaohong X; Gao, Xue X; Han, Mingyu M; Gao, Song S; Huang, Shasha S; Dai, Pu P
Publication Date: 2022-07

Variant appearance in text: rs1049982
PubMed Link: 35292975
Variant Present in the following documents:
  • AHG-86-207-s002.xlsx, sheet 1
View BVdb publication page



Genetic analysis of sinonasal undifferentiated carcinoma discovers recurrent SWI/SNF alterations and a novel PGAP3-SRPK1 fusion gene.

Bmc Cancer
Heft Neal, Molly E ME; Birkeland, Andrew C AC; Bhangale, Apurva D AD; Zhai, Jingyi J; Kulkarni, Aditi A; Foltin, Susan K SK; Jewell, Brittany M BM; Ludwig, Megan L ML; Pinatti, Lisa L; Jiang, Hui H; McHugh, Jonathan B JB; Marentette, Lawence L; McKean, Erin L EL; Brenner, J Chad JC
Publication Date: 2021-05-29

Variant appearance in text: rs1049982
PubMed Link: 34051734
Variant Present in the following documents:
  • 12885_2021_8370_MOESM15_ESM.xlsx, sheet 1
View BVdb publication page



Disseminated Talaromyces marneffei Infection in a Non-HIV Infant With a Homozygous Private Variant of RELB.

Frontiers In Cellular And Infection Microbiology
Ding, Xiaofang X; Huang, Han H; Zhong, Lili L; Chen, Min M; Peng, Fang F; Zhang, Bing B; Cui, Xinyu X; Yang, Xiu-An XA
Publication Date: 2021

Variant appearance in text: rs1049982
PubMed Link: 33791233
Variant Present in the following documents:
  • Table_2.xlsx, sheet 1
View BVdb publication page



Highly diversified core promoters in the human genome and their effects on gene expression and disease predisposition.

Bmc Genomics
Gupta, Hemant H; Chandratre, Khyati K; Sinha, Siddharth S; Huang, Teng T; Wu, Xiaobing X; Cui, Jian J; Zhang, Michael Q MQ; Wang, San Ming SM
Publication Date: 2020-11-30

Variant appearance in text: rs1049982
PubMed Link: 33256598
Variant Present in the following documents:
  • 12864_2020_7222_MOESM2_ESM.xlsx, sheet 3
  • 12864_2020_7222_MOESM2_ESM.xlsx, sheet 2
  • 12864_2020_7222_MOESM2_ESM.xlsx, sheet 22
View BVdb publication page



Next-generation sequencing identified novel Desmoplakin frame-shift variant in patients with Arrhythmogenic cardiomyopathy.

Bmc Cardiovascular Disorders
Lin, Xiaoping X; Ma, Yuankun Y; Cai, Zhejun Z; Wang, Qiyuan Q; Wang, Lihua L; Huo, Zhaoxia Z; Hu, Dan D; Wang, Jian'an J; Xiang, Meixiang M
Publication Date: 2020-02-11

Variant appearance in text: rs1049982
PubMed Link: 32046637
Variant Present in the following documents:
  • 12872_2020_1369_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page



Distinctive mutational spectrum and karyotype disruption in long-term cisplatin-treated urothelial carcinoma cell lines.

Scientific Reports
Skowron, Margaretha A MA; Petzsch, Patrick P; Hardt, Karin K; Wagner, Nicholas N; Beier, Manfred M; Stepanow, Stefanie S; Drechsler, Matthias M; Rieder, Harald H; Köhrer, Karl K; Niegisch, Günter G; Hoffmann, Michèle J MJ; Schulz, Wolfgang A WA
Publication Date: 2019-10-09

Variant appearance in text: rs1049982
PubMed Link: 31597922
Variant Present in the following documents:
  • 41598_2019_50891_MOESM3_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM2_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM5_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM9_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM7_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM6_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM4_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM8_ESM.xlsx, sheet 1
View BVdb publication page



Genetic polymorphisms associated with reactive oxygen species and blood pressure regulation.

The Pharmacogenomics Journal
Cuevas, Santiago S; Villar, Van Anthony M VAM; Jose, Pedro A PA
Publication Date: 2019-08

Variant appearance in text: rs1049982
PubMed Link: 30723314
Variant Present in the following documents:
  • Main text
  • nihms-1517349.pdf
View BVdb publication page



Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: rs1049982
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_5.xlsx, sheet 1
View BVdb publication page



A likely pathogenic variant putatively affecting splicing of PIGA identified in a multiple congenital anomalies hypotonia-seizures syndrome 2 (MCAHS2) family pedigree via whole-exome sequencing.

Molecular Genetics & Genomic Medicine
Yang, Junli J; Wang, Qiong Q; Zhuo, Qingcui Q; Tian, Huiling H; Li, Wen W; Luo, Fang F; Zhang, Jinghui J; Bi, Dan D; Peng, Jing J; Zhou, Dong D; Xin, Huawei H
Publication Date: 2018-09

Variant appearance in text: rs1049982
PubMed Link: 29974678
Variant Present in the following documents:
  • MGG3-6-739-s002.xlsx, sheet 7
  • MGG3-6-739-s002.xlsx, sheet 6
View BVdb publication page



RNAseq analysis of bronchial epithelial cells to identify COPD-associated genes and SNPs.

Bmc Pulmonary Medicine
Yeo, Jiyoun J; Morales, Diego A DA; Chen, Tian T; Crawford, Erin L EL; Zhang, Xiaolu X; Blomquist, Thomas M TM; Levin, Albert M AM; Massion, Pierre P PP; Arenberg, Douglas A DA; Midthun, David E DE; Mazzone, Peter J PJ; Nathan, Steven D SD; Wainz, Ronald J RJ; Nana-Sinkam, Patrick P; Willey, Paige F S PFS; Arend, Taylor J TJ; Padda, Karanbir K; Qiu, Shuhao S; Federov, Alexei A; Hernandez, Dawn-Alita R DR; Hammersley, Jeffrey R JR; Yoon, Youngsook Y; Safi, Fadi F; Khuder, Sadik A SA; Willey, James C JC
Publication Date: 2018-03-05

Variant appearance in text: rs1049982
PubMed Link: 29506519
Variant Present in the following documents:
  • Main text
View BVdb publication page



A Case-Control Study of the Genetic Variability in Reactive Oxygen Species-Metabolizing Enzymes in Melanoma Risk.

International Journal Of Molecular Sciences
Yuan, Tze-An TA; Yourk, Vandy V; Farhat, Ali A; Ziogas, Argyrios A; Meyskens, Frank L FL; Anton-Culver, Hoda H; Liu-Smith, Feng F
Publication Date: 2018-01-14

Variant appearance in text: rs1049982
PubMed Link: 29342889
Variant Present in the following documents:
  • Main text
  • ijms-19-00242.pdf
View BVdb publication page



Genetic polymorphisms of antioxidant enzymes CAT and SOD affect the outcome of clinical, biochemical, and anthropometric variables in people with obesity under a dietary intervention.

Genes & Nutrition
Hernández-Guerrero, César C; Parra-Carriedo, Alicia A; Ruiz-de-Santiago, Diana D; Galicia-Castillo, Oscar O; Buenrostro-Jáuregui, Mario M; Díaz-Gutiérrez, Carmen C
Publication Date: 2018

Variant appearance in text: rs1049982
PubMed Link: 29339975
Variant Present in the following documents:
  • Main text
View BVdb publication page



Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.

Oncotarget
Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH
Publication Date: 2017-11-10

Variant appearance in text: rs1049982
PubMed Link: 29221171
Variant Present in the following documents:
  • oncotarget-08-95841-s002.xlsx, sheet 1
  • oncotarget-08-95841-s002.xlsx, sheet 4
View BVdb publication page



Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.

Human Genome Variation
Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H
Publication Date: 2017

Variant appearance in text: rs1049982
PubMed Link: 28690861
Variant Present in the following documents:
  • hgv201727-s1.xls, sheet 1
View BVdb publication page



Analyses of antioxidant status and nucleotide alterations in genes encoding antioxidant enzymes in patients with benign and malignant thyroid disorders.

Peerj
Ramli, Nur Siti Fatimah NSF; Mat Junit, Sarni S; Leong, Ng Khoon NK; Razali, Nurhanani N; Jayapalan, Jaime Jacqueline JJ; Abdul Aziz, Azlina A
Publication Date: 2017

Variant appearance in text: rs1049982
PubMed Link: 28584708
Variant Present in the following documents:
  • Main text
  • peerj-05-3365.pdf
View BVdb publication page



Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.

Bmc Cancer
Lonjou, Christine C; Damiola, Francesca F; Moissonnier, Monika M; Durand, Geoffroy G; Malakhova, Irina I; Masyakin, Vladimir V; Le Calvez-Kelm, Florence F; Cardis, Elisabeth E; Byrnes, Graham G; Kesminiene, Ausrele A; Lesueur, Fabienne F
Publication Date: 2017-05-12

Variant appearance in text: rs1049982
PubMed Link: 28499365
Variant Present in the following documents:
  • 12885_2017_3314_MOESM1_ESM.xls, sheet 1
View BVdb publication page



NPR-C gene polymorphism is associated with increased susceptibility to coronary artery disease in Chinese Han population: a multicenter study.

Oncotarget
Hu, Qin Q; Liu, Qiji Q; Wang, Shasha S; Zhen, Xi X; Zhang, Zhimian Z; Lv, Ruijuan R; Jiang, Guihua G; Ma, Zhiyong Z; He, Hong H; Li, Daqing D; Liu, Xiaoling X; Gao, Fei F; Li, Jifu J; Li, Li L; Zhang, Mei M; Ji, Xiaoping X; Chen, Yuguo Y; Wang, Daowen D; Huang, Dejia D; Ma, Aiqun A; Huang, Wei W; Zhao, Yuxia Y; Gong, Yaoqin Y; Zhang, Cheng C; Zhang, Yun Y
Publication Date: 2016-06-07

Variant appearance in text: rs1049982
PubMed Link: 27191271
Variant Present in the following documents:
  • Main text
  • oncotarget-07-33662.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: rs1049982
PubMed Link: 26549847
Variant Present in the following documents:
  • mmc3.xlsx, sheet 3
  • mmc3.xlsx, sheet 1
  • mmc3.xlsx, sheet 2
View BVdb publication page



The nutrigenetic influence of the interaction between dietary vitamin E and TXN and COMT gene polymorphisms on waist circumference: a case control study.

Journal Of Translational Medicine
Mansego, Maria L ML; De Marco, Griselda G; Ivorra, Carmen C; Lopez-Izquierdo, Raúl R; Morcillo, Sonsoles S; Rojo-Martínez, Gemma G; González-Albert, Verónica V; Martinez, Fernando F; Soriguer, Federico F; Martín-Escudero, Juan C JC; Redon, Josep J; Chaves, F Javier FJ
Publication Date: 2015-09-02

Variant appearance in text: rs1049982
PubMed Link: 26329592
Variant Present in the following documents:
  • Main text
  • 12967_2015_Article_652.pdf
View BVdb publication page



Association of genetic variants with diabetic nephropathy.

World Journal Of Diabetes
Rizvi, Saliha S; Raza, Syed Tasleem ST; Mahdi, Farzana F
Publication Date: 2014-12-15

Variant appearance in text: rs1049982
PubMed Link: 25512783
Variant Present in the following documents:
  • Main text
View BVdb publication page



Oxidative stress in susceptibility to breast cancer: study in Spanish population.

Bmc Cancer
Rodrigues, Patricia P; de Marco, Griselda G; Furriol, Jessica J; Mansego, Maria Luisa ML; Pineda-Alonso, Mónica M; Gonzalez-Neira, Anna A; Martin-Escudero, Juan Carlos JC; Benitez, Javier J; Lluch, Ana A; Chaves, Felipe J FJ; Eroles, Pilar P
Publication Date: 2014-11-21

Variant appearance in text: rs1049982
PubMed Link: 25416100
Variant Present in the following documents:
  • Main text
  • 12885_2014_Article_5048.pdf
View BVdb publication page



Genetics of oxidative stress in obesity.

International Journal Of Molecular Sciences
Rupérez, Azahara I AI; Gil, Angel A; Aguilera, Concepción M CM
Publication Date: 2014-02-20

Variant appearance in text: rs1049982
PubMed Link: 24562334
Variant Present in the following documents:
  • Main text
  • ijms-15-03118.pdf
View BVdb publication page



The role of genetic polymorphisms in antioxidant enzymes and potential antioxidant therapies in neonatal lung disease.

Antioxidants & Redox Signaling
Dani, Carlo C; Poggi, Chiara C
Publication Date: 2014-11-01

Variant appearance in text: rs1049982
PubMed Link: 24382101
Variant Present in the following documents:
  • Main text
View BVdb publication page



Are catalase -844A/G polymorphism and activity associated with childhood obesity?

Antioxidants & Redox Signaling
Rupérez, Azahara I AI; Olza, Josune J; Gil-Campos, Mercedes M; Leis, Rosaura R; Mesa, María D MD; Tojo, Rafael R; Cañete, Ramón R; Gil, Angel A; Aguilera, Concepción M CM
Publication Date: 2013-12-01

Variant appearance in text: rs1049982
PubMed Link: 23641975
Variant Present in the following documents:
  • Main text
View BVdb publication page



Effects of polymorphisms in alcohol metabolism and oxidative stress genes on survival from head and neck cancer.

Cancer Epidemiology
Hakenewerth, Anne M AM; Millikan, Robert C RC; Rusyn, Ivan I; Herring, Amy H AH; Weissler, Mark C MC; Funkhouser, William K WK; North, Kari E KE; Barnholtz-Sloan, Jill S JS; Olshan, Andrew F AF
Publication Date: 2013-08

Variant appearance in text: rs1049982
PubMed Link: 23632049
Variant Present in the following documents:
  • Main text
View BVdb publication page



Progress in understanding the genetics of bronchopulmonary dysplasia.

Seminars In Perinatology
Shaw, Gary M GM; O'Brodovich, Hugh M HM
Publication Date: 2013-04

Variant appearance in text: rs1049982
PubMed Link: 23582962
Variant Present in the following documents:
  • Main text
View BVdb publication page



Polymorphism in glutamate cysteine ligase catalytic subunit (GCLC) is associated with sulfamethoxazole-induced hypersensitivity in HIV/AIDS patients.

Bmc Medical Genomics
Wang, Danxin D; Curtis, Amanda A; Papp, Audrey C AC; Koletar, Susan L SL; Para, Michael F MF
Publication Date: 2012-07-23

Variant appearance in text: rs1049982
PubMed Link: 22824134
Variant Present in the following documents:
  • Main text
  • 1755-8794-5-32.pdf
View BVdb publication page



Joint effects of alcohol consumption and polymorphisms in alcohol and oxidative stress metabolism genes on risk of head and neck cancer.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Hakenewerth, Anne M AM; Millikan, Robert C RC; Rusyn, Ivan I; Herring, Amy H AH; North, Kari E KE; Barnholtz-Sloan, Jill S JS; Funkhouser, William F WF; Weissler, Mark C MC; Olshan, Andrew F AF
Publication Date: 2011-11

Variant appearance in text: rs1049982
PubMed Link: 21940907
Variant Present in the following documents:
  • Main text
View BVdb publication page



Functional variants in the catalase and myeloperoxidase genes, ambient air pollution, and respiratory-related school absences: an example of epistasis in gene-environment interactions.

American Journal Of Epidemiology
Wenten, Madé M; Gauderman, W James WJ; Berhane, Kiros K; Lin, Pi-Chu PC; Peters, John J; Gilliland, Frank D FD
Publication Date: 2009-12-15

Variant appearance in text: rs1049982
PubMed Link: 19897513
Variant Present in the following documents:
  • Main text
View BVdb publication page



Detection of catalase as a major protein target of the lipid peroxidation product 4-HNE and the lack of its genetic association as a risk factor in SLE.

Bmc Medical Genetics
D'souza, Anil A; Kurien, Biji T BT; Rodgers, Rosalie R; Shenoi, Jaideep J; Kurono, Sadamu S; Matsumoto, Hiroyuki H; Hensley, Kenneth K; Nath, Swapan K SK; Scofield, R Hal RH
Publication Date: 2008-07-07

Variant appearance in text: rs1049982
PubMed Link: 18606005
Variant Present in the following documents:
  • Main text
View BVdb publication page



Interactions between genes involved in the antioxidant defence system and breast cancer risk.

British Journal Of Cancer
Oestergaard, M Z MZ; Tyrer, J J; Cebrian, A A; Shah, M M; Dunning, A M AM; Ponder, B A J BA; Easton, D F DF; Pharoah, P D P PD
Publication Date: 2006-08-21

Variant appearance in text: rs1049982
PubMed Link: 16868544
Variant Present in the following documents:
  • Main text
  • 95-6603272a.pdf
View BVdb publication page