Clinical and Genetic Characterization of Patients with Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Caused by a Plakophilin-2 Splice Mutation
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Title
Clinical and Genetic Characterization of Patients with Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Caused by a Plakophilin-2 Splice Mutation
Authors
Keywords
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Journal
CARDIOLOGY
Volume 123, Issue 3, Pages 181-189
Publisher
S. Karger AG
Online
2012-11-08
DOI
10.1159/000342717
References
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- (2010) Veronique Fressart et al. EUROPACE
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- Missense Variants in Plakophilin-2 in Arrhythmogenic Right Ventricular Cardiomyopathy Patients – Disease-Causing or Innocent Bystanders?
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- Comprehensive Desmosome Mutation Analysis in North Americans With Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy
- (2009) A. Dénise den Haan et al. Circulation-Cardiovascular Genetics
- Severe cardiac phenotype with right ventricular predominance in a large cohort of patients with a single missense mutation in the DES gene
- (2009) J. Peter van Tintelen et al. HEART RHYTHM
- A genetic variants database for arrhythmogenic right ventricular dysplasia/cardiomyopathy
- (2009) Paul A. van der Zwaag et al. HUMAN MUTATION
- Arrhythmogenic right ventricular cardiomyopathy
- (2009) Cristina Basso et al. LANCET
- A New Diagnostic Test for Arrhythmogenic Right Ventricular Cardiomyopathy
- (2009) Angeliki Asimaki et al. NEW ENGLAND JOURNAL OF MEDICINE
- Arrhythmogenic Right Ventricular Cardiomyopathy Type 5 Is a Fully Penetrant, Lethal Arrhythmic Disorder Caused by a Missense Mutation in the TMEM43 Gene
- (2008) Nancy D. Merner et al. AMERICAN JOURNAL OF HUMAN GENETICS
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