Lack of pancreatic body and tail in HNF1B mutation carriers

Diabetic Medicine

Volumn 25, Issue 7, 2008, Pages 782-787

  Haldorsen, I S ^a,b   Vesterhus, M ^a,b   Raeder H ^a,b   Jensen, D K ^a   Sovik O ^a,b   Molven, A ^a,b   Njolstad P R ^a,b  

^a HAUKELAND UNIVERSITY HOSPITAL   (Norway)

^b UNIVERSITY OF BERGEN   (Norway)

Author keywords

Genetics; Magnetic resonance imaging; Maturity onset diabetes of the young; Pancreatic function

Indexed keywords

ALPHA TOCOPHEROL; PANCREATIC ELASTASE; VITAMIN D; HEPATOCYTE NUCLEAR FACTOR 1BETA;

ADOLESCENT; ADULT; AGED; AGENESIS; ALPHA TOCOPHEROL DEFICIENCY; ARTICLE; CHILD; CLINICAL ARTICLE; COMPUTER ASSISTED TOMOGRAPHY; EXOCRINE GLAND; FEMALE; GENE; GENE MUTATION; GENE SEQUENCE; HEPATOCYTE NUCLEAR FACTOR 1BETA GENE; HETEROZYGOTE; HUMAN; MAGNETIC RESONANCE CHOLANGIOPANCREATOGRAPHY; MALE; PANCREAS; PANCREAS SECRETION; PHENOTYPE; PRESCHOOL CHILD; SCHOOL CHILD; VITAMIN BLOOD LEVEL; VITAMIN D DEFICIENCY; X RAY; CONGENITAL MALFORMATION; GENETICS; MIDDLE AGED; MUTATION; NON INSULIN DEPENDENT DIABETES MELLITUS; PATHOLOGY; PEDIGREE;

ADOLESCENT; ADULT; CHILD; DIABETES MELLITUS, TYPE 2; FEMALE; HEPATOCYTE NUCLEAR FACTOR 1-BETA; HETEROZYGOTE; HUMANS; MALE; MIDDLE AGED; MUTATION; PANCREAS; PANCREAS, EXOCRINE; PEDIGREE;

EID: 49649105254     PISSN: 07423071     EISSN: 14645491     Source Type: Journal    
DOI: 10.1111/j.1464-5491.2008.02460.x     Document Type: Article

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