Familial dilated cardiomyopathy with RBM20 mutation in an Indian patient: a case report
Abstract Background Dilated cardiomyopathy (DCM) is a disease of the heart muscle characterized by ventricular dilation and a left ventricular ejection fraction of less than 40%. Unlike hypertrophic cardiomyopathy (HCM) and arrhythmogenic right ventricular cardiomyopathy (ARVC), DCM-causing mutation...
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| Asıl Yazarlar: | , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
SpringerOpen
2021-05-01
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| Seri Bilgileri: | The Egyptian Heart Journal |
| Konular: | |
| Online Erişim: | https://doi.org/10.1186/s43044-021-00165-6 |
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