MYBPC3 gene variations in hypertrophic cardiomyopathy patients in India

BACKGROUND: Hypertrophic cardiomyopathy (HCM) is a complex cardiac muscular disorder, inherited as an autosomal dominant disease with variable penetrance. Cardiac myosin-binding protein C (MyBPC) is the predominant myosin-binding protein isoform in the heart muscle. One hundred forty-seven mutations...

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Detalhes bibliográficos
Main Authors: Tanjore, Reena R, Rangaraju, Advithi, Kerkar, PG, Calambur, Narsimhan, Nallari, Pratibha
Formato: Artigo
Idioma:Inglês
Publicado em: Pulsus Group Inc 2008
Assuntos:
Clinical Studies
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2644567/
https://ncbi.nlm.nih.gov/pubmed/18273486
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