HNF1B deletions in patients with young-onset diabetes but no known renal disease

Diabetic Medicine

Volumn 30, Issue 1, 2013, Pages 114-117

  Edghill, E L ^a   Stals, K ^b   Oram, R A ^a   Shepherd, M H ^a   Hattersley, A T ^a   Ellard, S ^a,b  

^a UNIVERSITY OF EXETER   (United Kingdom)

^b ROYAL DEVON AND EXETER NHS FOUNDATION TRUST   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

HEPATOCYTE NUCLEAR FACTOR 1BETA; INSULIN;

ADOLESCENT; ADULT; ARTICLE; CHILD; DIABETES MELLITUS; FAMILIAL DIABETES MELLITUS; FEMALE; FLUORESCENT POLYMERASE CHAIN REACTION ASSAY; GENE AMPLIFICATION; GENE DELETION; GENE MUTATION; GENETIC MARKER; GENETIC POLYMORPHISM; HETEROZYGOTE; HOMOZYGOTE; HUMAN; INSULIN TREATMENT; KIDNEY CYST; KIDNEY DEVELOPMENT; MAJOR CLINICAL STUDY; MALE; MOLECULAR PROBE; NON INSULIN DEPENDENT DIABETES MELLITUS; POLYMERASE CHAIN REACTION; RISK ASSESSMENT; SCHOOL CHILD;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; DIABETES MELLITUS, TYPE 2; DIABETIC NEPHROPATHIES; FEMALE; GENE DELETION; GENETIC TESTING; HEPATOCYTE NUCLEAR FACTOR 1-BETA; HOMOZYGOTE; HUMANS; INFANT; KIDNEY DISEASES, CYSTIC; MALE; MIDDLE AGED; POLYMORPHISM, GENETIC; YOUNG ADULT;

EID: 84871101188     PISSN: 07423071     EISSN: 14645491     Source Type: Journal    
DOI: 10.1111/j.1464-5491.2012.03709.x     Document Type: Article

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