High frequency of mutations in MODY and mitochondrial genes in Scandinavian patients with familial early-onset diabetes

Diabetologia

Volumn 42, Issue 9, 1999, Pages 1131-1137

  Lehto, M ^a,d   Wipemo, C ^a   Ivarsson, S A ^a   Lindgren, C ^a   Lipsanen Nyman, M ^b   Weng, J ^a   Wibell, L ^c   Widen E ^a   Tuomi, T ^a   Groop, L ^a  

^a LUND UNIVERSITY HOSPITAL   (Sweden)

^b HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

^c UPPSALA UNIVERSITY HOSPITAL   (Sweden)

^d MAS   (Sweden)

Author keywords

Genetics; Glucokinase; HNF 1; HNF 4; MIDD; MODY

Indexed keywords

GLUCOKINASE; LEUCINE TRANSFER RNA; MITOCHONDRIAL DNA; NUCLEAR FACTOR I;

ADULT; ARTICLE; CONTROLLED STUDY; FAMILIAL DISEASE; FEMALE; GENE FREQUENCY; GENE MUTATION; HUMAN; INSULIN DEPENDENT DIABETES MELLITUS; JUVENILE DIABETES MELLITUS; MAJOR CLINICAL STUDY; MALE; NON INSULIN DEPENDENT DIABETES MELLITUS; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM;

ADULT; AGE FACTORS; AGED; AGED, 80 AND OVER; BASIC HELIX-LOOP-HELIX LEUCINE ZIPPER TRANSCRIPTION FACTORS; DIABETES MELLITUS, TYPE 2; DNA, MITOCHONDRIAL; DNA-BINDING PROTEINS; EXONS; FAMILY; FEMALE; GLUCOKINASE; HEPATOCYTE NUCLEAR FACTOR 1; HEPATOCYTE NUCLEAR FACTOR 1-ALPHA; HEPATOCYTE NUCLEAR FACTOR 1-BETA; HEPATOCYTE NUCLEAR FACTOR 4; HUMANS; INTRONS; MALE; MIDDLE AGED; MUTATION; NUCLEAR PROTEINS; PEDIGREE; PHOSPHOPROTEINS; POINT MUTATION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; PROMOTER REGIONS (GENETICS); SCANDINAVIA; SEQUENCE DELETION; TRANSCRIPTION FACTORS; VARIATION (GENETICS);

EID: 0032857518     PISSN: 0012186X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s001250051281     Document Type: Article

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