Spectrum of Rare and Common Genetic Variants in Arrhythmogenic Cardiomyopathy Patients

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...

Full description

Bibliographic Details
Main Authors: Melania Lippi, Mattia Chiesa, Ciro Ascione, Matteo Pedrazzini, Saima Mushtaq, Davide Rovina, Daniela Riggio, Anna Maria Di Blasio, Maria Luisa Biondi, Giulio Pompilio, Gualtiero I. Colombo, Michela Casella, Valeria Novelli, Elena Sommariva
Format: Article
Language:English
Published: MDPI AG 2022-07-01
Series:Biomolecules
Subjects:
arrhythmogenic cardiomyopathy
cardiovascular genetics
genotype-phenotype correlation
desmosomal genes
rare variants
common variants
Online Access:https://www.mdpi.com/2218-273X/12/8/1043

Internet

https://www.mdpi.com/2218-273X/12/8/1043

Similar Items