A novel splice site mutation of the thiazide- sensitive NaCl cotransporter gene in a Japanese patient with Gitelman syndrome-Reference-Cited by-同舟云学术

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A novel splice site mutation of the thiazide- sensitive NaCl cotransporter gene in a Japanese patient with Gitelman syndrome

Published:2004-09-01 Issue:09 Volume:62 Page:180-184
ISSN:0301-0430
Container-title:Clinical Nephrology
language:en
Short-container-title:CN

Author:

Iida K.,Hanafusa M.,Maekawa I.,Kudo T.,Takahashi K.,Yoshioka S.,Kishimoto M.,Iguchi G.,Tsukamoto T.,Okimura Y.,Kaji H.,Chihara K.

Publisher

Dustri-Verlgag Dr. Karl Feistle

Subject

Nephrology,General Medicine

Cited by 6 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. Characterization of a Splicing Abnormality in Gitelman Syndrome;American Journal of Kidney Diseases;2008-06

2. A novel initial codon mutation of the thiazide-sensitive Na-Cl cotransporter gene in a Japanese patient with Gitelman's syndrome;Endocrine Journal;2008

3. The Cold, Hard Truth About Pediatric Research;Pediatric Research;2007-04

4. Detection of a Transcript Abnormality in mRNA of the SLC12A3 Gene Extracted From Urinary Sediment Cells of a Patient With Gitelman???s Syndrome;Pediatric Research;2007-04

5. Novel mutations in theSLC12A3gene causing Gitelman's syndrome in Swedes;DNA Sequence;2007-01

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