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Article

HNF1 alpha gene coding regions mutations screening, in a Caucasian population clinically characterized as MODY from Argentina.

Diabetes research and clinical practice - 1 Feb 2011

Lopez Ariel Pablo, Foscaldi Sabrina Andrea, Perez Maria Silvia, Rodriguez Martín, Traversa Mercedes, Puchulu Félix Miguel, Bergada Ignacio, Frechtel Gustavo Daniel

Abstract excerpt

INTRODUCTION: There are at least six subtypes of Maturity Onset Diabetes of the Young (MODY) with distinctive genetic causes. MODY 3 is caused by mutations in HNF1A gene, an insulin transcription factor, so mutations in this gene are associated with impaired insulin secretion. MODY 3 prevalence differs according to the population analyzed, but it is one of the most frequent subtypes. Therefore, our aims in this...

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Identifiers

PMID: 21168233
DOI: 10.1016/j.diabres.2010.11.024

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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