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Variations of the proprotein convertase subtilisin/kexin type 9 gene in coronary artery disease
OBJECTIVE: Coronary artery disease (CAD) is the principal cause of mortality and morbidity worldwide. Studies have provided controversial results regarding whether variations in the proprotein convertase subtilisin/kexin type 9 gene (PCSK9) are risk factors for CAD. In this study, we evaluated the r...
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| Publicado no: | J Int Med Res |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
SAGE Publications
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7140201/ https://ncbi.nlm.nih.gov/pubmed/30947598 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0300060519839519 |
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