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t/gene-clcn5

CLCN5 gene

Discuss publications and research concerning the CLCN5 gene.

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Related literature

A novel CLCN5 pathogenic mutation supports Dent disease with normal endosomal acidification.
CLCN5
A novel mutation of Dent's disease in an 11-year-old male with nephrolithiasis and nephrocalcinosis.
CLCN5
[Clinical and genetic analysis of Dent disease in 4 Chinese children].
CLCN5
Mutation Update of the CLCN5 Gene Responsible for Dent Disease 1.
CLCN5
Expanding the phenotype of proteinuria in Dent disease. A case series.
CLCN5
A novel CLCN5 mutation in a Chinese boy with Dent's disease.
CLCN5
Identification of a novel mutation in the CLCN5 gene in a Chinese family with Dent-1 disease.
CLCN5
A novel CLCN5 mutation in a boy with asymptomatic proteinuria and focal global glomerulosclerosis.
CLCN5
ClC-5 mutations associated with Dent's disease: a major role of the dimer interface.
CLCN5
OCRL1 mutation in a boy with Dent disease, mild mental retardation, but without cataracts.
CLCN5

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