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...

Descripción completa

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

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7700696/
https://www.ncbi.nlm.nih.gov/pubmed/33238575
http://dx.doi.org/10.3390/jcm9113781

Ejemplares similares