A variant at chromosome 9p21 is associated with recurrent myocardial infarction and cardiac death after acute coronary syndrome: The GRACE Genetics Study

AIMS: Recent genetic studies identified the rs1333049 variant on chromosome 9p21 as a major susceptibility locus for coronary artery disease and myocardial infarction (MI). Here, we evaluated whether this variant also contributes to recurrent MI or cardiac death following an acute coronary syndrome...

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Detalhes bibliográficos
Main Authors: Buysschaert, Ian, Carruthers, Kathryn F., Dunbar, Donald R., Peuteman, Gilian, Rietzschel, Ernst, Belmans, Ann, Hedley, Ann, De Meyer, Tim, Budaj, Andrzej, Van de Werf, Frans, Lambrechts, Diether, Fox, Keith A. A.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2010
Assuntos:
Clinical Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2862180/
https://ncbi.nlm.nih.gov/pubmed/20231156
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/eurheartj/ehq053
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