Familial Arrhythmogenic Cardiomyopathy: Clinical Determinants of Phenotype Discordance and the Impact of Endurance Sports

Arrhythmogenic cardiomyopathy (ACM) is primarily a familial disease with autosomal dominant inheritance. Incomplete penetrance and variable expression are common, resulting in diverse clinical manifestations. Although recent studies on genotype–phenotype relationships have improved our understanding...

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Detalles Bibliográficos
Autores principales: Costa, Sarah, Gasperetti, Alessio, Medeiros-Domingo, Argelia, Akdis, Deniz, Brunckhorst, Corinna, Saguner, Ardan M., Duru, Firat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7700696/
https://www.ncbi.nlm.nih.gov/pubmed/33238575
http://dx.doi.org/10.3390/jcm9113781

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