Exploring contractile protein mechanisms and target medications for cardiomyopathic patients with diastolic dysfunction

Abstract Genetic defects have been increasingly found in cardiomyopathies, which are often present with mutations in cardiac contractile proteins. These congenital defects involve numerous intracellular pathways and share several critical clinical features, such as systolic or diastolic dysfunction...

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Autors principals:	Dustin Gerber, Junjun Quan, Bo Pan, Xupei Huang, Jie Tian
Format:	Artigo
Idioma:	Inglês
Publicat:	Wiley 2024-03-01
Col·lecció:	Pediatric Discovery
Matèries:	cardiomyopathy diastolic dysfunction EGCG green tea extract mavacamten
Accés en línia:	https://doi.org/10.1002/pdi3.60
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