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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2023
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| Materias: | |
| 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 |