Rare Variants Associated with Arrhythmogenic Cardiomyopathy: Reclassification Five Years Later

Rare Variants Associated with Arrhythmogenic Cardiomyopathy: Reclassification Five Years Later

Genetic interpretation of rare variants associated with arrhythmogenic cardiomyopathy (ACM) is essential due to their diagnostic implications. New data may relabel previous variant classifications, but how often reanalysis is necessary remains undefined. Five years ago, 39 rare ACM-related variants...

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Bibliographic Details
Main Authors: Marta Vallverdú-Prats, Mireia Alcalde, Georgia Sarquella-Brugada, Sergi Cesar, Elena Arbelo, Anna Fernandez-Falgueras, Mónica Coll, Alexandra Pérez-Serra, Marta Puigmulé, Anna Iglesias, Victoria Fiol, Carles Ferrer-Costa, Bernat del Olmo, Ferran Picó, Laura Lopez, Paloma Jordà, Ana García-Álvarez, Coloma Tirón de Llano, Rocío Toro, Simone Grassi, Antonio Oliva, Josep Brugada, Ramon Brugada, Oscar Campuzano
Format: Article
Language:English
Published: MDPI AG 2021-02-01
Series:Journal of Personalized Medicine
Subjects:
sudden cardiac death
arrhythmogenic cardiomyopathy
genetics
rare variants
reclassification
Online Access:https://www.mdpi.com/2075-4426/11/3/162

Internet

https://www.mdpi.com/2075-4426/11/3/162

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