Cargando…
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...
| Autores principales: | , , , , , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Public Library of Science
2017
|
| Materias: | |
| 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 |