Atypical familial juvenile hyperuricemic nephropathy associated with a hepatocyte nuclear factor-1β gene mutation

Kidney International

Volumn 63, Issue 5, 2003, Pages 1645-1651

  Bingham, Coralie ^a   Ellard, Sian ^b   Van't Hoff, William G ^b   Simmonds, H Anne ^b   Marinaki, Anthony M ^b   Badman, Michael K ^b   Winocour, Peter H ^b   Stride, Amanda ^b   Lockwood, Christopher R ^b   Nicholls, Anthony J ^b   Owen, Katharine R ^b   Spyer, Ghislaine ^b   Pearson, Ewan R ^b   Hattersley, Andrew T ^b  

^a PENINSULA MEDICAL SCHOOL   (United Kingdom)

^b NONE

Author keywords

Familial renal disease; HNF 1 mutation; Hyperuricemia; Juvenile gout; Transcription factors

Indexed keywords

CREATININE; HEPATOCYTE NUCLEAR FACTOR 1BETA; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG; URATE;

ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 16; CHRONIC KIDNEY FAILURE; CLINICAL ARTICLE; FAMILIAL JUVENILE HYPERURICEMIC NEPHROPATHY; FEMALE; GENE MUTATION; GENETIC HETEROGENEITY; GOUT; HUMAN; HYPERURICEMIA; KIDNEY CYST; KIDNEY DEVELOPMENT; KIDNEY DISEASE; MALE; NON INSULIN DEPENDENT DIABETES MELLITUS; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; URIC ACID BLOOD LEVEL;

EID: 0037408284     PISSN: 00852538     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1523-1755.2003.00903.x     Document Type: Article

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