Characterization of a novel SCN5A mutation associated with long QT syndrome and arrhythmogenic right ventricular cardiomyopathy in a family
Author:
Funder
Guangzhou Science and Technology Project
National Key R&D Program of China
National Natural Science Foundation of China
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s12024-024-00863-y.pdf
Reference27 articles.
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2. Zheng JJ, Zheng D, Su T, et al. Sudden unexplained nocturnal death syndrome: the Hundred years’ Enigma. J Am Heart Assoc. 2018;7(5):30. https://doi.org/10.1161/JAHA.117.007837.
3. Hayashi M, Shimizu W, Albert CM. The spectrum of Epidemiology Underlying Sudden Cardiac Death. Circ Res. 2015;116(12):1887–906. https://doi.org/10.1161/CIRCRESAHA.116.304521.
4. Krahn AD, Wilde AAM, Calkins H, et al. Arrhythmogenic right ventricular cardiomyopathy. JACC-Clin Electrophy. 2022;8(4):533–53. https://doi.org/10.1016/j.jacep.2021.12.002.
5. Te Riele AS, Agullo-Pascual E, James CA, et al. Multilevel analyses of SCN5A mutations in arrhythmogenic right ventricular dysplasia/cardiomyopathy suggest non-canonical mechanisms for disease pathogenesis. Cardiovasc Res. 2017;113(1):102–11. https://doi.org/10.1093/cvr/cvw234.
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