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...

Полное описание

Библиографические подробности
Главные авторы: Lloyd, SE, Pearce, S, Günther, W, Kawaguchi, H, Igarashi, T, Jentsch, T, Thakker, R
Формат: Journal article
Язык:English
Опубликовано: 1997