Results 151 to 160 of about 10,292,350 (166)

Father-Daughter Autosomal Recessive Gitelman Syndrome Caused by Compound Heterozygous Variants in the SLC12A3 Gene.

Nephrology
Zhuo-Fan Zhang, Jing-Fang Han, Fang Wang, Xiao-Li Chen   +3 more
semanticscholar   +1 more source

[Analysis of novel mutations in the SLC12A3 gene of a family with Gitelman syndrome].

Zhonghua nei ke za zhi
J.-H. Zhang, H. Zhang, Wen-Li Ge, H.-Y. Yu, C. Hu, S. Chen   +5 more
semanticscholar   +1 more source

[Identification of pathological variants of SLC12A3 gene in a pedigree affected with Gitelman syndrome].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, 2020
Qian Ma, Jinlin Wu, L. Che, X. Kong
semanticscholar   +1 more source

Genetic Features of Chinese Patients With Gitelman Syndrome: Sixteen Novel SLC12A3 Mutations Identified in a New Cohort

American Journal of Nephrology, 2016
Ping-Yan Shen, Chunli Zhang
exaly  

Arg913Gln of SLC12A3 gene promotes development and progression of end-stage renal disease in Chinese type 2 diabetes mellitus

Molecular and Cellular Biochemistry, 2017
Rong Zhang, Lan-Gen Zhuang, Ming Li, Juan Zhang, Wei-Jing Zhao, Xiao-Xu Ge, Ya-Ting Chen, Feng Wang, Nian-Song Wang, Y. Bao, Limei Liu, Yan-Jun Liu, W. Jia   +12 more
semanticscholar   +1 more source

Novel SLC12A3 Mutations in Chinese Patients With Gitelman’s Syndrome

Nephron Physiology, 2008
Hong Ren, Weiming Wang, Leping Shao
exaly  

Gitelman Syndrome Caused by a Rare Homozygous Mutation in the SLC12A3 Gene: A Case Report

World Journal of Clinical Cases, 2020
Rizhen Yu, Maoshen Chen
exaly  

Novel Heterozygous Missense Mutation of SLC12A3 Gene in Gitelman Syndrome: A Case Report

World Journal of Clinical Cases, 2019
Chenglin Wang
exaly  

HAPLOTYPES IN THE WNK1 AND SLC12A3 GENES ARE ASSOCIATED TO HYPERTENSION IN A CHINESE POPULATION: 6B.02

Journal of Hypertension, 2010
S Wu, W Niu, Y Zhang, P Gao, X Jeunemaitre, D Zhu   +5 more
openaire   +1 more source

Identification of Fifteen Novel Mutations in the SLC12A3 Gene Encoding the Na-Cl Co-Transporter in Italian Patients With Gitelman Syndrome

Human Mutation, 2002
Domenico Coviello, Giorgio Casari, Alberto Edefonti   +2 more
exaly