Mutations of CLCN5 in Japanese children with idiopathic low molecular weight proteinuria, hypercalciuria and nephrocalcinosis-Reference-Cited by-同舟云学术

Mutations of CLCN5 in Japanese children with idiopathic low molecular weight proteinuria, hypercalciuria and nephrocalcinosis

Published:1997-10 Issue:4 Volume:52 Page:911-916
ISSN:0085-2538
Container-title:Kidney International
language:en
Short-container-title:Kidney International

Author:

Akuta Naoko,Lloyd Sarah E.,Igarashi Takashi,Shiraga Hiroshi,Matsuyama Takeshi,Yokoro Seitarou,Cox Jeremy P.D.,Thakker Rajesh V.

Publisher

Elsevier BV

Subject

Nephrology

Reference24 articles.

1. Hypercalciuria and nephrocalcinosis in patients with idiopathic low molecular weight proteinuria in Japan: Is this identical to Dent's disease in the United Kingdom;Igarashi;Nephron,1995

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

3. The clinical significance of asymptomatic low molecular weight proteinuria detected on routine screening of children in Japan: A survey of 53 patients;Murakami;Clin Nephrol,1990

4. Analysis of prognosis, renal histopathological findings and the hereditary basis of 17 patients with familial idiopathic low molecular weight proteinuria based on questionnaire (in Japanese);Furuse;Nihon Shounika Gakkaishi,1992

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

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