Myocardial Fibrosis in Hypertrophic Cardiomyopathy: A Perspective from Fibroblasts

Hypertrophic cardiomyopathy (HCM) is the most common inherited heart disease and the leading cause of sudden cardiac death in young people. Mutations in genes that encode structural proteins of the cardiac sarcomere are the more frequent genetic cause of HCM. The disease is characterized by cardiomy...

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Detalles Bibliográficos
Autores principales: Schlittler, Maja, Pramstaller, Peter P., Rossini, Alessandra, De Bortoli, Marzia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10573356/
https://www.ncbi.nlm.nih.gov/pubmed/37834293
http://dx.doi.org/10.3390/ijms241914845

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10573356/
https://www.ncbi.nlm.nih.gov/pubmed/37834293
http://dx.doi.org/10.3390/ijms241914845

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