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HNF1A gene polymorphisms and cardiovascular risk factors in individuals with late-onset autosomal dominant diabetes: a cross-sectional study

BACKGROUND: Type 2 diabetes mellitus (T2DM) is a genetically heterogeneous disease, hepatocyte nuclear factor-1 homeobox A (HNF1A) single-nucleotide polymorphisms (SNPs) playing a minor role in its pathogenesis. HNF1A is a frequent cause of monogenic diabetes, albeit with early-onset. Some uncommon...

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Detalles Bibliográficos
Autores principales: Giuffrida, Fernando MA, Furuzawa, Gilberto K, Kasamatsu, Teresa S, Oliveira, Marcos M, Reis, Andre F, Dib, Sergio A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2696421/
https://www.ncbi.nlm.nih.gov/pubmed/19490620
http://dx.doi.org/10.1186/1475-2840-8-28