A novel variant in plakophilin-2 gene detected in a family with arrhythmogenic right ventricular cardiomyopathy
Author:
Publisher
Springer Science and Business Media LLC
Subject
Physiology (medical),Cardiology and Cardiovascular Medicine
Link
http://link.springer.com/content/pdf/10.1007/s10840-011-9643-4.pdf
Reference26 articles.
1. Corrado, D., Basso, C., & Thiene, G. (2009). Arrhythmogenic right ventricular cardiomyopathy: an update. Heart, 95, 766–773.
2. Herren, T., Gerber, P. A., & Duru, F. (2009). Arrhythmogenic right ventricular cardiomyopathy/dysplasia: a not so rare "disease of the desmosome" with multiple clinical presentations. Clinical Research in Cardiology, 98, 141–158.
3. Hauer, R. N. (2009). Toward early diagnosis in arrhythmogenic right ventricular dysplasia/cardiomyopathy. Journal of Interventional Cardiac Electrophysiology, 26, 1–2.
4. Basso, C., Corrado, D., Marcus, F. I., Nava, A., & Thiene, G. (2009). Arrhythmogenic right ventricular cardiomyopathy. Lancet, 373, 1289–1300.
5. Sen-Chowdhry, S., Syrris, P., & McKenna, W. J. (2007). Role of genetic analysis in the management of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy. Journal of the American College of Cardiology, 50, 1813–1821.
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