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Article

Common variants in CASQ2, GPD1L, and NOS1AP are significantly associated with risk of sudden death in patients with coronary artery disease.

Circulation. Cardiovascular genetics - 1 Aug 2011

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

Abstract excerpt

BACKGROUND: 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. METHODS AND RESULTS: We investigated 1424 htSNPs representing 18 genes with mutations described in...

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Identifiers

PMID: 21685173
DOI: 10.1161/CIRCGENETICS.111.959916
PMCID: PMC3160237

Genes

SCD
CAD
CASQ2

Provenance

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