Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registry

BACKGROUND: Recent genome-wide association studies have identified several genetic loci linked to coronary artery disease (CAD) and myocardial infarction (MI). The 9p21.3 locus was verified by numerous replication studies to be the first common locus for CAD and MI. In the present study, we investig...

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Detalles Bibliográficos
Autores principales: Scheffold, Thomas, Kullmann, Silke, Huge, Andreas, Binner, Priska, Ochs, Hermann R, Schöls, Wolfgang, Thale, Joachim, Motz, Wolfgang, Hegge, Franz Josef, Stellbrink, Christoph, Dorsel, Thomas, Gülker, Hartmut, Heuer, Hubertus, Dinh, Wilfried, Stoll, Monika, Haltern, Georg
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3061953/
https://www.ncbi.nlm.nih.gov/pubmed/21385355
http://dx.doi.org/10.1186/1471-2261-11-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3061953/
https://www.ncbi.nlm.nih.gov/pubmed/21385355
http://dx.doi.org/10.1186/1471-2261-11-9

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