Novel Mutations in β-MYH7 Gene in Indian Patients With Dilated Cardiomyopathy

BACKGROUND: Heart failure is a hallmark of severe hypertrophic cardiomyopathy and dilated cardiomyopathy (DCM). Several mutations in the β-MYH7 gene lead to hypertrophic cardiomyopathy. Recently, causative mutations in the β-MYH7 gene have also been detected in DCM from different populations. METHOD...

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Detalles Bibliográficos
Autores principales: Rani, Deepa Selvi, Vijaya Kumar, Archana, Nallari, Pratibha, Sampathkumar, Katakam, Dhandapany, Perundurai S., Narasimhan, Calambur, Rathinavel, Andiappan, Thangaraj, Kumarasamy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8767027/
https://www.ncbi.nlm.nih.gov/pubmed/35072022
http://dx.doi.org/10.1016/j.cjco.2021.07.020

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8767027/
https://www.ncbi.nlm.nih.gov/pubmed/35072022
http://dx.doi.org/10.1016/j.cjco.2021.07.020

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