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

Journal of Clinical Investigation

Volumn 99, Issue 5, 1997, Pages 967-974

  Lloyd, S E ^a   Pearce, S H S ^a   Gunther W ^b   Kawaguchi, H ^c   Igarashi, T ^d   Jentsch, T J ^b   Thakker, R V ^a  

^a HAMMERSMITH HOSPITAL   (United Kingdom)

^b UNIVERSITY MEDICAL CENTER HAMBURG EPPENDORF   (Germany)

^c Department of Pediatrics   (Japan)

^d UNIVERSITY OF TOKYO   (Japan)

Author keywords

chloride channel mutations; hypercalciuria; proteinuria

Indexed keywords

CHLORIDE CHANNEL;

ADOLESCENT; ADULT; ANIMAL CELL; ARTICLE; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; DISEASE PREDISPOSITION; FEMALE; GENE EXPRESSION; GENE MUTATION; HUMAN; HYPERCALCIURIA; JAPAN; KIDNEY CALCIFICATION; KIDNEY TUBULE DISORDER; MALE; NONHUMAN; OOCYTE; PHENOTYPE; PRIORITY JOURNAL; PROTEINURIA; SCREENING TEST; SINGLE STRAND CONFORMATION POLYMORPHISM; URINALYSIS;

EID: 0030907872     PISSN: 00219738     EISSN: None     Source Type: Journal    
DOI: 10.1172/JCI119262     Document Type: Article

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