Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on Chromosome 17
Coronary artery disease (CAD) is a leading cause of death world-wide, and most cases have a complex, multifactorial aetiology that includes a substantial heritable component. Identification of new genes involved in CAD may inform pathogenesis and provide new therapeutic targets.The PROCARDIS study r...
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| Aineistotyyppi: | Journal article |
| Kieli: | English |
| Julkaistu: |
2006
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| Aiheet: |