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Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1 and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathy
BACKGROUND: Rare variants in >30 genes have been shown to cause idiopathic or familial dilated cardiomyopathy (IDC/FDC), but the frequency of genetic causation remains poorly understood. We have previously resequenced 9 genes in a cohort of IDC/FDC probands for rare variants, and now report reseq...
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| Hoofdauteurs: | , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2010
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2908892/ https://ncbi.nlm.nih.gov/pubmed/20215591 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCGENETICS.109.912345 |
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