Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5).

Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5).

The annual urinary screening of Japanese children above 3 yr of age has identified a progressive proximal renal tubular disorder characterized by low molecular weight proteinuria, hypercalciuria, and nephrocalcinosis. The disorder, which has a familial predisposition and occurs predominantly in male...

Bibliografske podrobnosti
Main Authors:	Lloyd, SE, Pearce, S, Günther, W, Kawaguchi, H, Igarashi, T, Jentsch, T, Thakker, R
Format:	Journal article
Jezik:	English
Izdano:	1997

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