An Update on MYBPC3 Gene Mutation in Hypertrophic Cardiomyopathy

An Update on MYBPC3 Gene Mutation in Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy (HCM) is the most prevalent genetically inherited cardiomyopathy that follows an autosomal dominant inheritance pattern. The majority of HCM cases can be attributed to mutation of the MYBPC3 gene, which encodes cMyBP-C, a crucial structural protein of the cardiac muscle....

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Bibliographic Details
Main Authors: Bogdan-Sorin Tudurachi, Alexandra Zăvoi, Andreea Leonte, Laura Țăpoi, Carina Ureche, Silviu Gabriel Bîrgoan, Traian Chiuariu, Larisa Anghel, Rodica Radu, Radu Andy Sascău, Cristian Stătescu
Format: Article
Language:English
Published: MDPI AG 2023-06-01
Series:International Journal of Molecular Sciences
Subjects:
hypertrophic cardiomyopathy (HCM)
MYBPC3
MYH7
genetic mutations
Online Access:https://www.mdpi.com/1422-0067/24/13/10510

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https://www.mdpi.com/1422-0067/24/13/10510

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