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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Veröffentlicht in:	International journal of molecular sciences 2023-10, Vol.24 (19), p.14845
Hauptverfasser:	Schlittler, Maja, Pramstaller, Peter P, Rossini, Alessandra, De Bortoli, Marzia
Format:	Artikel
Sprache:	eng
Schlagworte:	Cardiomyocytes Cardiomyopathy Cardiomyopathy, Hypertrophic Collagen Cytokines Disease Enzymes Fibroblasts Fibrosis Genes Genetic aspects Growth factors Heart Kinases Mutation Physiology Proteins Review Teenagers Transforming growth factors Youth
Online-Zugang:	Volltext
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