Familial dilated cardiomyopathy with RBM20 mutation in an Indian patient: a case report

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 mutations are pr...

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Detalles Bibliográficos
Autores principales: Das, Soumi, Seth, Sandeep
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8140951/
https://www.ncbi.nlm.nih.gov/pubmed/34021826
http://dx.doi.org/10.1186/s43044-021-00165-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8140951/
https://www.ncbi.nlm.nih.gov/pubmed/34021826
http://dx.doi.org/10.1186/s43044-021-00165-6

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