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[A Dutch family with an autosomal dominant form of diabetes mellitus as a result of a mutation in the HNF1 alpha-gene (MODY3)].

Nederlands tijdschrift voor geneeskunde - 10 Oct 1998

Tack C J, Hattersley A T

Abstract excerpt

OBJECTIVE: To study the molecular genetic basis of an autosomal dominant form of diabetes mellitus in a Dutch family. DESIGN: Descriptive. SETTING: Academic Hospital Nijmegen, the Netherlands and Laboratories for Molecular Genetics, Birmingham and Exeter, Great Britain. METHODS: A large pedigree with maturity-onset diabetes of the young (MODY) was studied by taking a history and by performing laboratory analysis;...

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PMID: 9864503

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[A Dutch family with an autosomal dominant form of diabetes mellitus as a result of a mutation in the HNF1 alpha-gene (MODY3)].PMID 9864503Read ↗

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Double heterozygous mutations involving both HNF1A/MODY3 and HNF4A/MODY1 genes: a case report.Semantic proximity Read ↗

The HNF1A mutant Ala180Val: Clinical challenges in determining causality of a rare HNF1A variant in familial diabetes.Semantic proximity Read ↗

[Mutations in the genes of the HNF-family cause maturity-onset diabetes of the young (MODY)].Semantic proximity Read ↗

Clinical characteristics and diagnostic criteria of maturity-onset diabetes of the young (MODY) due to molecular anomalies of the HNF1A gene.Semantic proximity Read ↗

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The spectrum of HNF1A gene mutations in Greek patients with MODY3: relative frequency and identification of seven novel germline mutations.Semantic proximity Read ↗

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

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