Yanhua Lang

Identification of seven exonic variants in the <i>SLC4A1</i> , <i>ATP6V1B1</i> , and <i>ATP6V0A4</i> genes that alter RNA splicing by minigene assay

Ruixiao Zhang, Zeqing Chen, Qijing Song et al. · Human Mutation · 2021 · 45 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Genotype/Phenotype Analysis in 67 Chinese Patients with Gitelman's Syndrome

Ting Liu, Cui Wang, Jingru Lu et al. · American Journal of Nephrology · 2016 · 43 citations

Medicine, Genetics, Molecular Genetics +17

A novel SLC4A1 variant in an autosomal dominant distal renal tubular acidosis family with a severe phenotype

Leping Shao, Yan Xu, Qian Dong et al. · Endocrine · 2010 · 26 citations

Medicine, Molecular Genetics, Nephrology +11

Coexistence of normotensive primary aldosteronism in two patients with Gitelman's syndrome and novel thiazide-sensitive Na–Cl cotransporter mutations

Zhimin Miao, Yufang Gao, René J.M. Bindels et al. · European Journal of Endocrinology · 2009 · 26 citations · Full text

Life Sciences, Endocrinology, Genetics +12

A Novel SLC12A3 Splicing Mutation Skipping of Two Exons and Preliminary Screening for Alternative Splice Variants in Human Kidney

Leping Shao, Zhimin Miao, Hong Ren et al. · American Journal of Nephrology · 2008 · 25 citations

Medicine, Endocrinology, Molecular Genetics +16