Functional genetic variants within the SIRT2 gene promoter in acute myocardial infarction

Coronary artery disease (CAD), including acute myocardial infarction (AMI) is the complication of atherosclerosis. Recently, genome-wide association studies have identified a large number of CAD-related genetic variants. However, only 10% of CAD cases could be explained. Low frequent and rare geneti...

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Detalles Bibliográficos
Autores principales: Yang, Wentao, Gao, Feng, Zhang, Pei, Pang, Shuchao, Cui, Yinghua, Liu, Lixin, Wei, Guanghe, Yan, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5406008/
https://www.ncbi.nlm.nih.gov/pubmed/28445509
http://dx.doi.org/10.1371/journal.pone.0176245

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5406008/
https://www.ncbi.nlm.nih.gov/pubmed/28445509
http://dx.doi.org/10.1371/journal.pone.0176245

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