Potential new mechanisms of pro-arrhythmia in arrhythmogenic cardiomyopathy: focus on calcium sensitive pathways
Author:
Funder
CVON-PREDICT
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine
Link
http://link.springer.com/content/pdf/10.1007/s12471-017-0946-7.pdf
Reference50 articles.
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3. van Tintelen JP, Entius MM, Bhuiyan ZA, et al. Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy. Circulation. 2006;113:1650–8.
4. Cuenca S, Ruiz-Cano MJ, Gimeno-Blanes JR, et al. Genetic Basis of Familial Dilated Cardiomyopathy Undergoing Heart Transplantation. J Heart Lung Transplant. 2016;35:625–35.
5. Cerrone M, Noorman M, Lin X, et al. Sodium current deficit and arrhythmogenesis in a murine model of plakophilin-2 haploinsufficiency. Cardiovasc Res. 2012;95:460–8.
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