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Common variants at 9p21 are associated with sudden and arrhythmic cardiac death
BACKGROUND: While a heritable basis for sudden cardiac death (SCD) is suggested by the impact of family history on SCD risk, genetic determinants have been difficult to identify. We hypothesized that a common variant at chromosome 9p21 related to myocardial infarction would influence SCD risk. METHO...
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| Glavni autori: | , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2009
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2785227/ https://ncbi.nlm.nih.gov/pubmed/19901189 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCULATIONAHA.109.879049 |
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