Genetic, clinical, molecular, and pathogenic aspects of the South Asian–specific polymorphic MYBPC3(Δ25bp) variant

Hypertrophic cardiomyopathy (HCM) is a cardiac genetic disease characterized by ventricular enlargement, diastolic dysfunction, and increased risk for sudden cardiac death. Sarcomeric genetic defects are the predominant known cause of HCM. In particular, mutations in the myosin-binding protein C gen...

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Detalhes bibliográficos
Publicado no:Biophys Rev
Main Authors: Arif, Mohammed, Nabavizadeh, Pooneh, Song, Taejeong, Desai, Darshini, Singh, Rohit, Bazrafshan, Sholeh, Kumar, Mohit, Wang, Yigang, Gilbert, Richard J., Dhandapany, Perundurai S., Becker, Richard C., Kranias, Evangelia G., Sadayappan, Sakthivel
Formato: Artigo
Idioma:Inglês
Publicado em: Springer Berlin Heidelberg 2020
Assuntos:
Review
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7429610/
https://ncbi.nlm.nih.gov/pubmed/32656747
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12551-020-00725-1
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