Common Variants in CASQ2, GPD1L, and NOS1APAre Significantly Associated With Risk of Sudden Death in Patients With Coronary Artery Disease
| Title: | Common Variants in CASQ2, GPD1L, and NOS1APAre Significantly Associated With Risk of Sudden Death in Patients With Coronary Artery Disease |
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| Authors: | Westaway, Shawn K., Reinier, Kyndaron, Huertas-Vazquez, Adriana, Evanado, Audrey, Teodorescu, Carmen, Navarro, Jo, Sinner, Moritz F., Gunson, Karen, Jui, Jonathan, Spooner, Peter, Kaab, Stefan, Chugh, Sumeet S. |
| Source: | Circulation: Cardiovascular Genetics; August 2011, Vol. 4 Issue: 4 p397-402, 6p |
| Abstract: | Recent evidence suggests a genetic component for sudden cardiac death (SCD) in subjects with coronary artery disease (CAD). We conducted a systematic candidate-gene approach using haplotype-tagging single nucleotide polymorphisms (htSNPs) to identify genes associated with SCD risk in the context of CAD. |
| Database: | Supplemental Index |
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