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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Detalles Bibliográficos
Autores principales: Tudurachi, Bogdan-Sorin, Zăvoi, Alexandra, Leonte, Andreea, Țăpoi, Laura, Ureche, Carina, Bîrgoan, Silviu Gabriel, Chiuariu, Traian, Anghel, Larisa, Radu, Rodica, Sascău, Radu Andy, Stătescu, Cristian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10341819/
https://www.ncbi.nlm.nih.gov/pubmed/37445689
http://dx.doi.org/10.3390/ijms241310510

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10341819/
https://www.ncbi.nlm.nih.gov/pubmed/37445689
http://dx.doi.org/10.3390/ijms241310510

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