Sudden Death and Left Ventricular Involvement in Arrhythmogenic Cardiomyopathy
Published 2019 View Full Article
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Title
Sudden Death and Left Ventricular Involvement in Arrhythmogenic Cardiomyopathy
Authors
Keywords
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Journal
CIRCULATION
Volume -, Issue -, Pages -
Publisher
Ovid Technologies (Wolters Kluwer Health)
Online
2019-01-31
DOI
10.1161/circulationaha.118.037230
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Note: Only part of the references are listed.- Desmoplakin missense and non-missense mutations in arrhythmogenic right ventricular cardiomyopathy: Genotype-phenotype correlation
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- HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies: This document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA)
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- Arrhythmogenic Right Ventricular Cardiomyopathy Type 5 Is a Fully Penetrant, Lethal Arrhythmic Disorder Caused by a Missense Mutation in the TMEM43 Gene
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- Left-Dominant Arrhythmogenic Cardiomyopathy
- (2008) Srijita Sen-Chowdhry et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
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