Genotype-phenotype relationship in patients with arrhythmogenic right ventricular cardiomyopathy caused by desmosomal gene mutations: A systematic review and meta-analysis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/srep41387.pdf
Reference43 articles.
1. Meurs, K. M. et al. Genome-wide association identifies a deletion in the 3′ untranslated region of striatin in a canine model of arrhythmogenic right ventricular cardiomyopathy. Hum Genet 128, 315–324, doi: 10.1007/s00439-010-0855-y (2010).
2. Corrado, D. et al. Trends in sudden cardiovascular death in young competitive athletes after implementation of a preparticipation screening program. JAMA 296, 1593–1601, doi: 10.1001/jama.296.13.1593 (2006).
3. Marcus, F. I., Edson, S. & Towbin, J. A. Genetics of arrhythmogenic right ventricular cardiomyopathy: a practical guide for physicians. J Am Coll Cardiol 61, 1945–1948, doi: 10.1016/j.jacc.2013.01.073 (2013).
4. Roux-Buisson, N. et al. Prevalence and significance of rare RYR2 variants in arrhythmogenic right ventricular cardiomyopathy/dysplasia: results of a systematic screening. Heart Rhythm 11, 1999–2009, doi: 10.1016/j.hrthm.2014.07.020 (2014).
5. van der Zwaag, P. A. et al. Phospholamban R14del mutation in patients diagnosed with dilated cardiomyopathy or arrhythmogenic right ventricular cardiomyopathy: evidence supporting the concept of arrhythmogenic cardiomyopathy. Eur J Heart Fail 14, 1199–1207, doi: 10.1093/eurjhf/hfs119 (2012).
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