Abstract
Sudden cardiac death (SCD) from ventricular fibrillation during myocardial infarction is a leading cause of total and cardiovascular mortality. It has a multifactorial, complex nature and aggregates in families, implicating the involvement of heritable factors in the determination of risk. During the last few years, genome-wide association studies have uncovered common genetic variants modulating risk of SCD. We here review the current insight on genetic determinants of SCD in the community and describe the genome-wide association approaches undertaken thus far in uncovering genetic determinants of SCD risk
Original language | English |
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Pages (from-to) | 6864-6872 |
Journal | Current pharmaceutical design |
Volume | 19 |
Issue number | 39 |
DOIs | |
Publication status | Published - 2013 |