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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Vydáno v:J Int Med Res
Hlavní autoři: Chiang, Shih-Min, Yang, Yi-Sun, Yang, Shun-Fa, Tsai, Chin-Feng, Ueng, Kwo-Chnag
Médium: Artigo
Jazyk:Inglês
Vydáno: SAGE Publications 2019
Témata:
Special Issue: Advances in Cardiometabolic and Coronary Artery Disease
On-line přístup: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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