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

Abstract:
AIMS/HYPOTHESIS: To investigate the contribution of mutations in maturity-onset diabetes of the young (MODY) and mitochondrial genes to early-onset diabetes with a strong family history of diabetes in a cohort with a high prevalence of Type I (insulin-dependent) diabetes mellitus. METHODS: Screening for sequence variants in the hepatocyte nuclear factor (HNF)-4alpha (MODY1), glucokinase (MODY2), HNF-1alpha (MODY3) genes and mitochondrial DNA was carried out in 115 Finnish and Swedish patients with early-onset (
Publication status:
Published

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Publisher copy:
10.1007/s001250051281

Authors


Ivarsson, SA More by this author
Lindgren, C More by this author
Lipsanen-Nyman, M More by this author
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Journal:
Diabetologia
Volume:
42
Issue:
9
Pages:
1131-1137
Publication date:
1999-09-05
DOI:
EISSN:
1432-0428
ISSN:
0012-186X
URN:
uuid:d9e74282-3c76-4e1c-93c4-8d61530c0467
Source identifiers:
22104
Local pid:
pubs:22104

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