Spectrum of Rare and Common Genetic Variants in Arrhythmogenic Cardiomyopathy Patients

Arrhythmogenic cardiomyopathy (ACM) is a rare inherited disorder, whose genetic cause is elusive in about 50–70% of cases. ACM presents a variable disease course which could be influenced by genetics. We performed next-generation sequencing on a panel of 174 genes associated with inherited cardiovas...

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Detalles Bibliográficos
Autores principales: Lippi, Melania, Chiesa, Mattia, Ascione, Ciro, Pedrazzini, Matteo, Mushtaq, Saima, Rovina, Davide, Riggio, Daniela, Di Blasio, Anna Maria, Biondi, Maria Luisa, Pompilio, Giulio, Colombo, Gualtiero I., Casella, Michela, Novelli, Valeria, Sommariva, Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9405889/
https://www.ncbi.nlm.nih.gov/pubmed/36008935
http://dx.doi.org/10.3390/biom12081043

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9405889/
https://www.ncbi.nlm.nih.gov/pubmed/36008935
http://dx.doi.org/10.3390/biom12081043

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