Mutations in the CLCN5 gene in Japanese patients with familial idiopathic low-molecular-weight proteinuria-Reference-Cited by-同舟云学术

Mutations in the CLCN5 gene in Japanese patients with familial idiopathic low-molecular-weight proteinuria

Published:1997-10 Issue:4 Volume:52 Page:895-900
ISSN:0085-2538
Container-title:Kidney International
language:en
Short-container-title:Kidney International

Author:

Nakazato Hitoshi,Hattori Shinzaburo,Furuse Akio,Kawano Tomoyasu,Karashima Shinnyo,Tsuruta Motoko,Yoshimuta Junichiro,Endo Fumio,Matsuda Ichiro

Publisher

Elsevier BV

Subject

Nephrology

Reference17 articles.

1. Asymptomatic low molecular weight proteinuria: A report on 5 cases;Suzuki;Clin Nephrol,1985

2. Asymptomatic Low Molecular Weight Proteinuria: Studies In Five Patients;Murakami;Clin Nephrol,1987

3. Familial progressive renal tubulopathy;Furuse;Clin Nephrol,1992

4. Dent's disease; A familial proximal renal tubular syndrome with low-molecular-weight proteinuria, hypercalciuria, nephrocalcinosis, metabolic bone disease, progressive renal failure and a marked male predominance;Wrong;Quart J Med,1994

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

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