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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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| Asıl Yazarlar: | , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2010
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| Konular: | |
| Online Erişim: | 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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