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Genetic and Functional Sequence Variants of the SIRT3 Gene Promoter in Myocardial Infarction
Coronary artery disease (CAD), including myocardial infarction (MI), is a common complex disease that is caused by atherosclerosis. Although a large number of genetic variants have been associated with CAD, only 10% of CAD cases could be explained. It has been proposed that low frequent and rare gen...
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| Publicado no: | PLoS One |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4831762/ https://ncbi.nlm.nih.gov/pubmed/27078640 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0153815 |
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