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...

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Detalles Bibliográficos
Autores principales: Farrall, Martin, Green, Fiona R, Peden, John F, Olsson, Per G, Clarke, Robert, Hellenius, Mai-Lis, Rust, Stephan, Lagercrantz, Jacob, Franzosi, Maria Grazia, Schulte, Helmut, Carey, Alisoun, Olsson, Gunnar, Assmann, Gerd, Tognoni, Gianni, Collins, Rory, Hamsten, Anders, Watkins, Hugh
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2006
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1463045/
https://www.ncbi.nlm.nih.gov/pubmed/16710446
http://dx.doi.org/10.1371/journal.pgen.0020072

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1463045/
https://www.ncbi.nlm.nih.gov/pubmed/16710446
http://dx.doi.org/10.1371/journal.pgen.0020072

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