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ANGPTL3 Deficiency and Protection Against Coronary Artery Disease
BACKGROUND: Familial combined hypolipidemia, a Mendelian condition characterized by substantial reductions in all 3 major lipid fractions, is caused by mutations that inactivate the gene angiopoietin-like 3 (ANGPTL3). Whether ANGPTL3 deficiency reduces risk of coronary artery disease (CAD) is unknow...
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| 發表在: | J Am Coll Cardiol |
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
2017
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5404817/ https://ncbi.nlm.nih.gov/pubmed/28385496 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jacc.2017.02.030 |
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