Common genetic variants on chromosome 9p21 are associated with myocardial infarction and type 2 diabetes in an Italian population

BACKGROUND: A genomic region on chromosome 9p21 has been identified as closely associated with increased susceptibility to coronary artery disease (CAD) and to type 2 diabetes (T2D) although the evidence suggests that the genetic variants within chromosome 9p21 that contribute to CAD are different f...

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Detalhes bibliográficos
Main Authors: Gori, Francesca, Specchia, Claudia, Pietri, Silvia, Crociati, Luisa, Barlera, Simona, Franciosi, Monica, Nicolucci, Antonio, Signorini, Stefano, Brambilla, Paolo, Franzosi, Maria Grazia
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2010
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Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2871267/
https://ncbi.nlm.nih.gov/pubmed/20403154
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-11-60
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