Transcriptional and Functional Analyses ofSLC12A3Mutations: New Clues for the Pathogenesis of Gitelman Syndrome-Reference-Cited by-同舟云学术

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Transcriptional and Functional Analyses ofSLC12A3Mutations: New Clues for the Pathogenesis of Gitelman Syndrome

Published:2007-02-28 Issue:4 Volume:18 Page:1271-1283
ISSN:1046-6673
Container-title:Journal of the American Society of Nephrology
language:en
Short-container-title:JASN

Author:

Riveira-Munoz Eva,Chang Qing,Godefroid Nathalie,Hoenderop Joost G.,Bindels René J.,Dahan Karin,Devuyst Olivier

Publisher

American Society of Nephrology (ASN)

Subject

Nephrology,General Medicine

Reference45 articles.

1. Genetic Variants of Thiazide-Sensitive NaCl-Cotransporter in Gitelman’s Syndrome and Primary Hypertension

2. Gitelman's variant of Barter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na–Cl cotransporter

3. Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome with predominant localization to the C-terminal domain

4. Gitelman's syndrome revisited: An evaluation of symptoms and health-related quality of life

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1. Navigating the multifaceted intricacies of the Na⁺-Cl⁻ cotransporter, a highly regulated key effector in the control of hydromineral homeostasis;Physiological Reviews;2024-07-01

2. A 23-year-old woman with metabolic alkalosis and hypokalemia;Canadian Medical Association Journal;2024-06-09

3. Genotype–phenotype correlations in children with Gitelman syndrome;Clinical and Experimental Nephrology;2024-03-13

4. Diagnosis, Treatment and Follow-Up Analysis of a Case of Gitelman Syndrome in Adolescents;Advances in Clinical Medicine;2024

5. Novel compound heterozygous variants of SLC12A3 gene in a Chinese patient with Gitelman syndrome: a case report;Frontiers in Genetics;2023-06-12

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