Clinical and Molecular Data Define a Diagnosis of Arrhythmogenic Cardiomyopathy in a Carrier of a Brugada-Syndrome-Associated PKP2 Mutation

Plakophilin-2 (PKP2) is the most frequently mutated desmosomal gene in arrhythmogenic cardiomyopathy (ACM), a disease characterized by structural and electrical alterations predominantly affecting the right ventricular myocardium. Notably, ACM cases without overt structural alterations are frequentl...

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Detalhes bibliográficos
Publicado no:Genes (Basel)
Main Authors: Persampieri, Simone, Pilato, Chiara Assunta, Sommariva, Elena, Maione, Angela Serena, Stadiotti, Ilaria, Ranalletta, Antonio, Torchio, Margherita, Dello Russo, Antonio, Basso, Cristina, Pompilio, Giulio, Tondo, Claudio, Casella, Michela
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI 2020
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7288341/
https://ncbi.nlm.nih.gov/pubmed/32443836
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes11050571
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