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Article

T130I mutation in HNF-4α gene is a loss-of-function mutation in hepatocytes and is associated with late-onset Type 2 diabetes mellitus in Japanese subjects

25 Mar 2003

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 12669197
DOI: 10.1007/s00125-003-1067-y

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T130I mutation in HNF-4α gene is a loss-of-function mutation in hepatocytes and is associated with late-onset Type 2 diabetes mellitus in Japanese subjectsPMID 12669197Read ↗

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The Landscape of HNF1B Deficiency: A Syndrome Not Yet Fully ExploredSemantic proximity Read ↗

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Thr130Ile polymorphism of HNF4A gene is associated with gestational diabetes mellitus in Mexican population.Semantic proximity Read ↗

[HNF-1alpha G319S mutation in Oji-Cree type 2 diabetes].Semantic proximity Read ↗

Exploring the role of the HNF-1αG319S polymorphism in β cell failure and youth-onset type 2 diabetes: Lessons from MODY and Hnf-1α-deficient animal models.Semantic proximity Read ↗

Identification of HNF4A Mutation p.T130I and HNF1A Mutations p.I27L and p.S487N in a Han Chinese Family with Early-Onset Maternally Inherited Type 2 Diabetes.Semantic proximity Read ↗

Phenotypic heterogeneity in Chinese patients with hepatocyte nuclear factor-1β mutations.Semantic proximity Read ↗

Early-onset type 2 diabetes mellitus is associated to HNF4A T130I polymorphism in families of central Spain.Semantic proximity Read ↗

Identification of a gain-of-function mutation in the HNF-1beta gene in a Japanese family with MODY.Semantic proximity Read ↗

Mutation in the HNF-4alpha gene affects insulin secretion and triglyceride metabolism.Semantic proximity Read ↗

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