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Article

Letter Re: Neonatal diabetes mellitus and mutation in the HNF-1beta gene.

The Journal of clinical endocrinology and metabolism - 1 Oct 2005

D'Amato Elena, Lorini Renata

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Share to Diabetes Mellitus
Share to DNA-Binding Proteins
Share to Hepatocyte Nuclear Factor 1-beta
Share to Infant, Newborn

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 16207896
DOI: 10.1210/jc.2005-1156

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Letter Re: Neonatal diabetes mellitus and mutation in the HNF-1beta gene.PMID 16207896Read ↗

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A novel phenotype of a hepatocyte nuclear factor homeobox A (HNF1A) gene mutation, presenting with neonatal cholestasis.Semantic proximity Read ↗

Commentary: The mutations and clinical variability in maternally inherited diabetes and deafness: an analysis of 161 patients.Semantic proximity Read ↗

A description of a fetal syndrome associated with HNF1B mutation and a wide intrafamilial disease variability.Semantic proximity Read ↗

Hepatocyte nuclear factor-1 beta mutations cause neonatal diabetes and intrauterine growth retardation: support for a critical role of HNF-1beta in human pancreatic development.Semantic proximity Read ↗

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

Congenital hyperinsulinism due to mutations in HNF4A and HADH.Semantic proximity Read ↗

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MNX1 mutations causing neonatal diabetes: Review of the literature and report of a case with extra-pancreatic congenital defects presenting in severe diabetic ketoacidosis.Semantic proximity Read ↗

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