CLCN5 chloride-channel mutations in six new North American families with X-linked nephrolithiasis-Reference-Cited by-同舟云学术

CLCN5 chloride-channel mutations in six new North American families with X-linked nephrolithiasis

Published:1998-09 Issue:3 Volume:54 Page:698-705
ISSN:0085-2538
Container-title:Kidney International
language:en
Short-container-title:Kidney International

Author:

Hoopes Richard R.,Hueber Paul A.,Reid Robert J.,Braden Gregory L.,Goodyer Paul R.,Melnyk Andrew R.,Midgley Julian P.,Moel Donald I.,Neu Alicia M.,VanWhy Scott K.,Scheinman Steven J.

Publisher

Elsevier BV

Subject

Nephrology

Reference19 articles.

1. X-linked hypercalciuric nephrolithiasis: Clinical syndromes and chloride channel mutations;Scheinman;Kidney Int,1998

2. A common molecular basis for three inherited kidney stone diseases;Lloyd;Nature,1996

3. Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5);Lloyd;J Clin Invest,1997

4. Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders;Lloyd;Hum Molec Genet,1997

5. X-linked recessive nephrolithiasis with renal failure;Frymoyer;N Engl J Med,1991

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