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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...
Autores principales: | Chiang, Shih-Min, Yang, Yi-Sun, Yang, Shun-Fa, Tsai, Chin-Feng, Ueng, Kwo-Chnag |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7140201/ https://www.ncbi.nlm.nih.gov/pubmed/30947598 http://dx.doi.org/10.1177/0300060519839519 |
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