Atypical Gitelman syndrome with L623P mutation of the thiazide-sensitive Na-Cl cotransporter gene exhibiting lack of hypocalciuria and increased proximal tubule salt reabsorption-Reference-Cited by-同舟云学术

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Atypical Gitelman syndrome with L623P mutation of the thiazide-sensitive Na-Cl cotransporter gene exhibiting lack of hypocalciuria and increased proximal tubule salt reabsorption

Published:2006-09-12 Issue:11 Volume:21 Page:3340-3341
ISSN:0931-0509
Container-title:Nephrology Dialysis Transplantation
language:en
Short-container-title:Nephrology Dialysis Transplantation

Author:

Mizumori Y.,Muto S.,Uchida S.-i.,Sasaki S.,Kusano E.

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Link

http://academic.oup.com/ndt/article-pdf/21/11/3340/7987055/gfl361.pdf

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Chasing Electrolytes After a Diagnosis of Disordered Eating;Clinical Pediatrics;2018-12-29

2. Adaptation in Gitelman Syndrome: “We Just Want to Pump You Up”;Clinical Journal of the American Society of Nephrology;2012-02-16

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