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Common susceptibility variants examined for association with dilated cardiomyopathy

BACKGROUND: Rare mutations in more than 20 genes have been suggested to cause dilated cardiomyopathy (DCM), but explain only a small percentage of cases, mainly in familial forms. We hypothesized that more common variants may also play a role in increasing genetic susceptibility to DCM, similar to t...

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Detalhes bibliográficos
Main Authors: Rampersaud, Evadnie, Kinnamon, Daniel D., Hamilton, Kara, Khuri, Sawsan, Hershberger, Ray E., Martin, Eden R.
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2866200/
https://ncbi.nlm.nih.gov/pubmed/20201937
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1469-1809.2010.00566.x
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