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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Detalles Bibliográficos
Autores principales: Gori, Francesca, Specchia, Claudia, Pietri, Silvia, Crociati, Luisa, Barlera, Simona, Franciosi, Monica, Nicolucci, Antonio, Signorini, Stefano, Brambilla, Paolo, Franzosi, Maria Grazia
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2871267/
https://www.ncbi.nlm.nih.gov/pubmed/20403154
http://dx.doi.org/10.1186/1471-2350-11-60

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2871267/
https://www.ncbi.nlm.nih.gov/pubmed/20403154
http://dx.doi.org/10.1186/1471-2350-11-60

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