1. Doundoulakis, Ioannis, Pannone, Luigi, Chiotis, Sotirios, Chierchia, Gian Battista, de Asmundis, Carlo. 2024. SCN5A gene variants and arrhythmic risk in Brugada syndrome: An updated systematic review and meta-analysis. In Heart rhythm, 21, 1987-1997. doi:10.1016/j.hrthm.2024.04.047. https://pubmed.ncbi.nlm.nih.gov/38614189/
2. Deica, Andreea Valentina, Paduraru, Livia Florentina, Paduraru, Dan Nicolae, Andronic, Octavian. 2022. The SCN5A Gene Is a Predictor of Phenotype Severity in Brugada Syndrome: A Comprehensive Literature Review. In Medical principles and practice : international journal of the Kuwait University, Health Science Centre, 32, 1-8. doi:10.1159/000528375. https://pubmed.ncbi.nlm.nih.gov/36446338/
3. Zaklyazminskaya, Elena, Dzemeshkevich, Sergei. 2016. The role of mutations in the SCN5A gene in cardiomyopathies. In Biochimica et biophysica acta, 1863, 1799-805. doi:10.1016/j.bbamcr.2016.02.014. https://pubmed.ncbi.nlm.nih.gov/26916278/
4. Raharjo, Sunu Budhi, Maulana, Rido, Maghfirah, Irma, Hanafy, Dicky A, Yuniadi, Yoga. 2018. SCN5A gene mutations and the risk of ventricular fibrillation and syncope in Brugada syndrome patients: A meta-analysis. In Journal of arrhythmia, 34, 473-477. doi:10.1002/joa3.12097. https://pubmed.ncbi.nlm.nih.gov/30327691/
5. Veerman, Christiaan C, Wilde, Arthur A M, Lodder, Elisabeth M. 2015. The cardiac sodium channel gene SCN5A and its gene product NaV1.5: Role in physiology and pathophysiology. In Gene, 573, 177-87. doi:10.1016/j.gene.2015.08.062. https://pubmed.ncbi.nlm.nih.gov/26361848/
6. Porretta, Alessandra P, Probst, Vincent, Bhuiyan, Zahurul A, Superti-Furga, Andrea, Pruvot, Etienne. 2022. SCN5A overlap syndromes: An open-minded approach. In Heart rhythm, 19, 1363-1368. doi:10.1016/j.hrthm.2022.03.1223. https://pubmed.ncbi.nlm.nih.gov/35351625/
智鼠故事 
