Publications:

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Recent Progress in Genetics and Epigenetics Research on Diabetic Nephropathy in Malaysia.

Journal Of Diabetes Research

Abu Seman, Norhashimah N; Othman, Siti Haslina SH

Publication Date: 2023

Variant appearance in text: rs11643718

PubMed Link: 37187702

Variant Present in the following documents:

• JDR2023-9053580.pdf

View BVdb publication page

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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: rs11643718

PubMed Link: 36241656

Variant Present in the following documents:

• 41598_2022_20939_MOESM15_ESM.xlsx, sheet 2

View BVdb publication page

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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: rs11643718

PubMed Link: 36075891

Variant Present in the following documents:

• 41439_2022_208_MOESM4_ESM.xlsx, sheet 2
• 41439_2022_208_MOESM5_ESM.xlsx, sheet 2

View BVdb publication page

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SLC12A3 Variation and Renal Function in Chinese Patients With Hypertension.

Frontiers In Medicine

Huang, Chin-Chou CC; Chung, Chia-Min CM; Yang, Chih-Yu CY; Leu, Hsin-Bang HB; Huang, Po-Hsun PH; Lin, Liang-Yu LY; Wu, Tao-Cheng TC; Lin, Shing-Jong SJ; Pan, Wen-Harn WH; Chen, Jaw-Wen JW

Publication Date: 2022

Variant appearance in text: rs11643718

PubMed Link: 35801212

Variant Present in the following documents:

• fmed-09-863275.pdf

View BVdb publication page

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Integrated DNA and RNA Sequencing Reveals Drivers of Endocrine Resistance in Estrogen Receptor-Positive Breast Cancer.

Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research

Xia, Youli Y; He, Xiaping X; Renshaw, Lorna L; Martinez-Perez, Carlos C; Kay, Charlene C; Gray, Mark M; Meehan, James J; Parker, Joel S JS; Perou, Charles M CM; Carey, Lisa A LA; Dixon, J Michael JM; Turnbull, Arran A

Publication Date: 2022-08-15

Variant appearance in text: rs11643718

PubMed Link: 35653148

Variant Present in the following documents:

• ccr-21-3189_supplementary_tables_ts1-9_suppts1-9.xlsx, sheet 5

View BVdb publication page

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Genetic and Biological Effects of SLC12A3, a Sodium-Chloride Cotransporter, in Gitelman Syndrome and Diabetic Kidney Disease.

Frontiers In Genetics

Li, Nan N; Gu, Harvest F HF

Publication Date: 2022

Variant appearance in text: SLC12A3: Arg904Gln

PubMed Link: 35591852

Variant Present in the following documents:

• Main text
• fgene-13-799224.pdf

View BVdb publication page

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Neoadjuvant PD-1 Blockade Combined With Chemotherapy Followed by Concurrent Immunoradiotherapy in Locally Advanced Anal Canal Squamous Cell Carcinoma Patients: Antitumor Efficacy, Safety and Biomarker Analysis.

Frontiers In Immunology

Xiao, WeiWei W; Yuan, Yan Y; Wang, SuiHai S; Liao, Zhidong Z; Cai, PeiQiang P; Chen, BaoQing B; Zhang, Rong R; Wang, Fang F; Zeng, ZhiFan Z; Gao, YuanHong Y

Publication Date: 2021

Variant appearance in text: SLC12A3: R904Q

PubMed Link: 35095878

Variant Present in the following documents:

• Table_2.xlsx, sheet 1

View BVdb publication page

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Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto's Thyroiditis Caused by Compound Heterozygous SLC12A3 Mutations.

Biomed Research International

Zhang, Jian-Hui JH; Ruan, Dan-Dan DD; Hu, Ya-Nan YN; Ruan, Xing-Lin XL; Zhu, Yao-Bin YB; Yang, Xiao X; Wu, Jia-Bin JB; Lin, Xin-Fu XF; Luo, Jie-Wei JW; Tang, Fa-Qiang FQ

Publication Date: 2021

Variant appearance in text: SLC12A3: 2711G>A; rs11643718

PubMed Link: 34046503

Variant Present in the following documents:

• Main text
• BMRI2021-9973161.pdf

View BVdb publication page

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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: rs11643718

PubMed Link: 33791233

Variant Present in the following documents:

• Table_2.xlsx, sheet 1

View BVdb publication page

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Integrated genetic and metabolic landscapes predict vulnerabilities of temozolomide resistant glioblastoma cells.

Npj Systems Biology And Applications

Immanuel, Selva Rupa Christinal SRC; Ghanate, Avinash D AD; Parmar, Dharmeshkumar S DS; Yadav, Ritu R; Uthup, Riya R; Panchagnula, Venkateswarlu V; Raghunathan, Anu A

Publication Date: 2021-01-08

Variant appearance in text: SLC12A3: R904Q; rs11643718

PubMed Link: 33420045

Variant Present in the following documents:

• 41540_2020_161_MOESM3_ESM.xlsx, sheet 2
• 41540_2020_161_MOESM3_ESM.xlsx, sheet 4
• 41540_2020_161_MOESM3_ESM.xlsx, sheet 3

View BVdb publication page

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Association of MMP-9 polymorphisms with diabetic nephropathy risk: A protocol for systematic review and meta-analysis.

Medicine

Xie, Yan Y; Wang, Zhixue Z; Chang, Lin L; Chen, Guotao G

Publication Date: 2020-09-18

Variant appearance in text: rs11643718

PubMed Link: 32957381

Variant Present in the following documents:

• medi-99-e22278.pdf

View BVdb publication page

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The single nucleotide polymorphism rs11643718 in SLC12A3 is associated with the development of diabetic kidney disease in Chinese people with type 2 diabetes.

Diabetic Medicine : A Journal Of The British Diabetic Association

Yang, J-F JF; Xiong, X-F XF; Xiao, Y Y; Wei, L L; Li, L L; Yang, M M; Han, Y-C YC; Zhao, H H; Li, C-R CR; Jiang, N N; Xiong, S S; Zeng, L-F LF; Zhou, Z-G ZG; Liu, S-P SP; Wang, N-S NS; Fan, Y Y; Sun, L L

Publication Date: 2020-11

Variant appearance in text: rs11643718

PubMed Link: 32634861

Variant Present in the following documents:

• Main text

View BVdb publication page

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A novel loss-of-function mutation of PBK associated with human kidney stone disease.

Scientific Reports

Nettuwakul, Choochai C; Sawasdee, Nunghathai N; Praditsap, Oranud O; Rungroj, Nanyawan N; Pasena, Arnat A; Dechtawewat, Thanyaporn T; Deejai, Nipaporn N; Sritippayawan, Suchai S; Rojsatapong, Santi S; Chaowagul, Wipada W; Yenchitsomanus, Pa-Thai PT

Publication Date: 2020-06-24

Variant appearance in text: rs11643718

PubMed Link: 32581305

Variant Present in the following documents:

• 41598_2020_66936_MOESM1_ESM.pdf

View BVdb publication page

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Multi-level evidence of an allelic hierarchy of USH2A variants in hearing, auditory processing and speech/language outcomes.

Communications Biology

Perrino, Peter A PA; Talbot, Lidiya L; Kirkland, Rose R; Hill, Amanda A; Rendall, Amanda R AR; Mountford, Hayley S HS; Taylor, Jenny J; , ; Buscarello, Alexzandrea N AN; Lahiri, Nayana N; Saggar, Anand A; Fitch, R Holly RH; Newbury, Dianne F DF

Publication Date: 2020-04-20

Variant appearance in text: rs11643718

PubMed Link: 32313182

Variant Present in the following documents:

• 42003_2020_885_MOESM2_ESM.xlsx, sheet 1

View BVdb publication page

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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: rs11643718

PubMed Link: 32046637

Variant Present in the following documents:

• 12872_2020_1369_MOESM1_ESM.xlsx, sheet 1

View BVdb publication page

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PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.

Genome Biology

Zhang, Chao C; Gao, Yang Y; Ning, Zhilin Z; Lu, Yan Y; Zhang, Xiaoxi X; Liu, Jiaojiao J; Xie, Bo B; Xue, Zhe Z; Wang, Xiaoji X; Yuan, Kai K; Ge, Xueling X; Pan, Yuwen Y; Liu, Chang C; Tian, Lei L; Wang, Yuchen Y; Lu, Dongsheng D; Hoh, Boon-Peng BP; Xu, Shuhua S

Publication Date: 2019-10-22

Variant appearance in text: rs11643718

PubMed Link: 31640808

Variant Present in the following documents:

• 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1

View BVdb publication page

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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: SLC12A3: R904Q; rs11643718

PubMed Link: 31597922

Variant Present in the following documents:

• 41598_2019_50891_MOESM5_ESM.xlsx, sheet 1
• 41598_2019_50891_MOESM4_ESM.xlsx, sheet 1

View BVdb publication page

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Polymorphisms in PCSK9, LDLR, BCMO1, SLC12A3, and KCNJ1 are Associated with Serum Lipid Profile in Chinese Han Population.

International Journal Of Environmental Research And Public Health

Li, Zheng Z; Zhao, Tianyu T; Tan, Xiaohua X; Lei, Song S; Huang, Liu L; Yang, Lei L

Publication Date: 2019-09-02

Variant appearance in text: rs11643718

PubMed Link: 31480784

Variant Present in the following documents:

• Main text
• ijerph-16-03207.pdf

View BVdb publication page

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Genetic Analysis of SLC12A3 Gene in Chinese Patients with Gitelman Syndrome.

Medical Science Monitor : International Medical Journal Of Experimental And Clinical Research

Zeng, Yanmei Y; Li, Ping P; Fang, Shu S; Wu, Chunyan C; Zhang, Yudan Y; Lin, Xiaochun X; Guan, Meiping M

Publication Date: 2019-08-09

Variant appearance in text: SLC12A3: Arg904Gln

PubMed Link: 31398183

Variant Present in the following documents:

• Main text
• medscimonit-25-5942.pdf

View BVdb publication page

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Genetic and Epigenetic Studies in Diabetic Kidney Disease.

Frontiers In Genetics

Gu, Harvest F HF

Publication Date: 2019

Variant appearance in text: rs11643718

PubMed Link: 31231424

Variant Present in the following documents:

• Main text
• fgene-10-00507.pdf

View BVdb publication page

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Establishment and genomic characterization of gingivobuccal carcinoma cell lines with smokeless tobacco associated genetic alterations and oncogenic PIK3CA mutation.

Scientific Reports

Pansare, Kshama K; Gardi, Nilesh N; Kamat, Sayee S; Dange, Prerana P; Previn, Rahul R; Gera, Poonam P; Kowtal, Pradnya P; Amin, Kishore K; Sarin, Rajiv R

Publication Date: 2019-06-04

Variant appearance in text: SLC12A3: R904Q; rs11643718

PubMed Link: 31164688

Variant Present in the following documents:

• 41598_2019_44143_MOESM2_ESM.xls, sheet 1

View BVdb publication page

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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: rs11643718

PubMed Link: 30894629

Variant Present in the following documents:

• 41598_2019_41277_MOESM4_ESM.xlsx, sheet 9
• 41598_2019_41277_MOESM4_ESM.xlsx, sheet 12

View BVdb publication page

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Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases.

Cell Death & Disease

Grassi, Ludovica L; Alfonsi, Romina R; Francescangeli, Federica F; Signore, Michele M; De Angelis, Maria Laura ML; Addario, Antonio A; Costantini, Manuela M; Flex, Elisabetta E; Ciolfi, Andrea A; Pizzi, Simone S; Bruselles, Alessandro A; Pallocca, Matteo M; Simone, Giuseppe G; Haoui, Mustapha M; Falchi, Mario M; Milella, Michele M; Sentinelli, Steno S; Di Matteo, Paola P; Stellacci, Emilia E; Gallucci, Michele M; Muto, Giovanni G; Tartaglia, Marco M; De Maria, Ruggero R; Bonci, Désirée D

Publication Date: 2019-02-27

Variant appearance in text: rs11643718

PubMed Link: 30814510

Variant Present in the following documents:

• 41419_2019_1453_MOESM27_ESM.xlsx, sheet 1

View BVdb publication page

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The Susceptibility Genes in Diabetic Nephropathy.

Kidney Diseases (Basel, Switzerland)

Wei, Ling L; Xiao, Ying Y; Li, Li L; Xiong, Xiaofen X; Han, Yachun Y; Zhu, Xuejing X; Sun, Lin L

Publication Date: 2018-11

Variant appearance in text: rs11643718

PubMed Link: 30574499

Variant Present in the following documents:

• Main text

View BVdb publication page

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Hypokalemia, hypomagnesemia, hypocalciuria, and recurrent tetany: Gitelman syndrome in a Chinese pedigree and literature review.

Clinical Case Reports

Xia, Ming-Feng MF; Bian, Hua H; Liu, Hong H; Wu, Hui-Juan HJ; Zhang, Zhi-Gang ZG; Lu, Zhi-Qiang ZQ; Gao, Xin X

Publication Date: 2017-05

Variant appearance in text: SLC12A3: R904Q

PubMed Link: 28469853

Variant Present in the following documents:

• Main text
• CCR3-5-578.pdf

View BVdb publication page

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Three-dimensional modelling identifies novel genetic dependencies associated with breast cancer progression in the isogenic MCF10 model.

The Journal Of Pathology

Maguire, Sarah L SL; Peck, Barrie B; Wai, Patty T PT; Campbell, James J; Barker, Holly H; Gulati, Aditi A; Daley, Frances F; Vyse, Simon S; Huang, Paul P; Lord, Christopher J CJ; Farnie, Gillian G; Brennan, Keith K; Natrajan, Rachael R

Publication Date: 2016-11

Variant appearance in text: SLC12A3: R904Q; rs11643718

PubMed Link: 27512948

Variant Present in the following documents:

• PATH-240-315-s015.xlsx, sheet 1

View BVdb publication page

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Assessing the Relationship of Angiotensin II Type 1 Receptors with Erythropoietin in a Human Model of Endogenous Angiotensin II Type 1 Receptor Antagonism.

Cardiorenal Medicine

Calò, Lorenzo A LA; Davis, Paul A PA; Maiolino, Giuseppe G; Pagnin, Elisa E; Ravarotto, Verdiana V; Naso, Elena E; Carraro, Gianni G; Naso, Agostino A

Publication Date: 2015-12

Variant appearance in text: SLC12A3: Arg904Gln

PubMed Link: 27194993

Variant Present in the following documents:

• Main text

View BVdb publication page

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Reproducible Analysis of Post-Translational Modifications in Proteomes--Application to Human Mutations.

Plos One

Holehouse, Alex S AS; Naegle, Kristen M KM

Publication Date: 2015

Variant appearance in text: rs11643718

PubMed Link: 26659599

Variant Present in the following documents:

• pone.0144692.s002.xlsx, sheet 1

View BVdb publication page

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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: SLC12A3: R904Q; rs11643718

PubMed Link: 26549847

Variant Present in the following documents:

• mmc3.xlsx, sheet 1
• mmc3.xlsx, sheet 3
• mmc3.xlsx, sheet 2

View BVdb publication page

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Relationship between NOX4 level and angiotensin II signaling in Gitelman's syndrome. Implications with hypertension.

International Journal Of Clinical And Experimental Medicine

Calò, Lorenzo A LA; Savoia, Carmine C; Davis, Paul A PA; Pagnin, Elisa E; Ravarotto, Verdiana V; Maiolino, Giuseppe G

Publication Date: 2015

Variant appearance in text: SLC12A3: Arg904Gln

PubMed Link: 26221292

Variant Present in the following documents:

• Main text

View BVdb publication page

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Gender-based differences on the association between salt-sensitive genes and obesity in Korean children aged between 8 and 9 years.

Plos One

Lee, Myoungsook M; Kim, Mi Kyung MK; Kim, Seon-Mee SM; Park, Hyesoon H; Park, Chang Gyu CG; Park, Hye Kyung HK

Publication Date: 2015

Variant appearance in text: SLC12A3: Arg904Gln

PubMed Link: 25768006

Variant Present in the following documents:

• Main text
• pone.0120111.pdf

View BVdb publication page

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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: SLC12A3: R904Q; rs11643718

PubMed Link: 25390934

Variant Present in the following documents:

• pone.0112430.s004.xlsx, sheet 1

View BVdb publication page

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Extracellular water and blood pressure in adults with growth hormone (GH) deficiency: a genotype-phenotype association study.

Plos One

Barbosa, Edna J L EJ; Glad, Camilla A M CA; Nilsson, Anna G AG; Bosaeus, Niklas N; Nyström, Helena Filipsson HF; Svensson, Per-Arne PA; Bengtsson, Bengt-Åke BÅ; Nilsson, Staffan S; Bosaeus, Ingvar I; Boguszewski, Cesar Luiz CL; Johannsson, Gudmundur G

Publication Date: 2014

Variant appearance in text: rs11643718

PubMed Link: 25157616

Variant Present in the following documents:

• Main text
• pone.0105754.pdf

View BVdb publication page

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NCI-60 whole exome sequencing and pharmacological CellMiner analyses.

Plos One

Reinhold, William C WC; Varma, Sudhir S; Sousa, Fabricio F; Sunshine, Margot M; Abaan, Ogan D OD; Davis, Sean R SR; Reinhold, Spencer W SW; Kohn, Kurt W KW; Morris, Joel J; Meltzer, Paul S PS; Doroshow, James H JH; Pommier, Yves Y

Publication Date: 2014

Variant appearance in text: rs11643718

PubMed Link: 25032700

Variant Present in the following documents:

• pone.0101670.s004.xlsx, sheet 1

View BVdb publication page

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Identifying common genetic variants in blood pressure due to polygenic pleiotropy with associated phenotypes.

Hypertension (Dallas, Tex. : 1979)

Andreassen, Ole A OA; McEvoy, Linda K LK; Thompson, Wesley K WK; Wang, Yunpeng Y; Reppe, Sjur S; Schork, Andrew J AJ; Zuber, Verena V; Barrett-Connor, Elizabeth E; Gautvik, Kaare K; Aukrust, Pål P; Karlsen, Tom H TH; Djurovic, Srdjan S; Desikan, Rahul S RS; Dale, Anders M AM; ,

Publication Date: 2014-04

Variant appearance in text: rs11643718

PubMed Link: 24396023

Variant Present in the following documents:

• Main text

View BVdb publication page

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Identification of autoimmune gene signatures in autism.

Translational Psychiatry

Jung, J-Y JY; Kohane, I S IS; Wall, D P DP

Publication Date: 2011-12-13

Variant appearance in text: rs11643718

PubMed Link: 22832355

Variant Present in the following documents:

• Main text

View BVdb publication page

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Spectrum of mutations in Gitelman syndrome.

Journal Of The American Society Of Nephrology : Jasn

Vargas-Poussou, Rosa R; Dahan, Karin K; Kahila, Diana D; Venisse, Annabelle A; Riveira-Munoz, Eva E; Debaix, Huguette H; Grisart, Bernard B; Bridoux, Franck F; Unwin, Robert R; Moulin, Bruno B; Haymann, Jean-Philippe JP; Vantyghem, Marie-Christine MC; Rigothier, Claire C; Dussol, Bertrand B; Godin, Michel M; Nivet, Hubert H; Dubourg, Laurence L; Tack, Ivan I; Gimenez-Roqueplo, Anne-Paule AP; Houillier, Pascal P; Blanchard, Anne A; Devuyst, Olivier O; Jeunemaitre, Xavier X

Publication Date: 2011-04

Variant appearance in text: rs11643718

PubMed Link: 21415153

Variant Present in the following documents:

• Main text

View BVdb publication page

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Promoter Polymorphism of RGS2 Gene Is Associated with Change of Blood Pressure in Subjects with Antihypertensive Treatment: The Azelnidipine and Temocapril in Hypertensive Patients with Type 2 Diabetes Study.

International Journal Of Hypertension

Sugimoto, Ken K; Katsuya, Tomohiro T; Kamide, Kei K; Fujisawa, Tomomi T; Shimaoka, Izumi I; Ohishi, Mitsuru M; Morishita, Ryuichi R; Ogihara, Toshio T; Rakugi, Hiromi H

Publication Date: 2010-08-24

Variant appearance in text: SLC12A3: Arg904Gln; rs11643718

PubMed Link: 20981351

Variant Present in the following documents:

• Main text
• IJHT2010-196307.pdf

View BVdb publication page

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