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...
প্রধান লেখক: | Lloyd, SE, Pearce, S, Günther, W, Kawaguchi, H, Igarashi, T, Jentsch, T, Thakker, R |
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বিন্যাস: | Journal article |
ভাষা: | English |
প্রকাশিত: |
1997
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অনুরূপ উপাদানগুলি
অনুরূপ উপাদানগুলি
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Hypercalciuric nephrocalcinosis in Japanese children due to mutations of the renal chloride channel (CLCN5).
অনুযায়ী: Lloyd, SE, অন্যান্য
প্রকাশিত: (1996) -
Mutations of CLCN5 in Japanese children with idiopathic low molecular weight proteinuria, hypercalciuria and nephrocalcinosis.
অনুযায়ী: Akuta, N, অন্যান্য
প্রকাশিত: (1997) -
Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders.
অনুযায়ী: Lloyd, SE, অন্যান্য
প্রকাশিত: (1997) -
Mutations in the chloride channel gene (CLCN5) are associated with hypercalciuric rickets and nephrolithiasis.
অনুযায়ী: Lloyd, SE, অন্যান্য
প্রকাশিত: (1996) -
Functional characterization of renal chloride channel, CLCN5, mutations associated with Dent'sJapan disease.
অনুযায়ী: Igarashi, T, অন্যান্য
প্রকাশিত: (1998)