Mutation Analysis of Three Exons of Myosin-Binding Protein C3 in Patients with Hypertrophic Cardiomyopathy

Background: Hypertrophic cardiomyopathy is a genetic disorder with a prevalence rate of 0.2% in the general population. It comes from mutations in sarcomeric proteins. Cardiac myosin-binding protein C3 is one of the critical genes in hypertrophic cardiomyopathy (HCM) and sudden cardiac death, accoun...

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Detalles Bibliográficos
Autores principales: Mobasheri, Maryam Beigom, Modarressi, Mohammad Hossein, Darabian, Cirus, Zeinalou, Ali Akbar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences, 2006- 2016
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5148813/
https://www.ncbi.nlm.nih.gov/pubmed/27956910

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5148813/
https://www.ncbi.nlm.nih.gov/pubmed/27956910

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