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Identification of Novel Mutations in RBM20 in Patients with Dilated Cardiomyopathy
The genetic basis of most of dilated cardiomyopathy (DCM) cases remains unknown. A recent study indicated that mutations in a highly localized five amino acid hotspot in exon 9 of RBM20, a gene encoding a ribonucleic acid‐binding protein, caused aggressive DCM. We undertook this study to confi rm an...
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| Asıl Yazarlar: | , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Blackwell Publishing Inc
2010
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2898174/ https://ncbi.nlm.nih.gov/pubmed/20590677 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1752-8062.2010.00198.x |
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