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. Kapoor, Ashish, Lee, Dongwon, Zhu, Luke, Arking, Dan E, Chakravarti, Aravinda. 2019. Multiple SCN5A variant enhancers modulate its cardiac gene expression and the QT interval. In Proceedings of the National Academy of Sciences of the United States of America, 116, 10636-10645. doi:10.1073/pnas.1808734116. https://pubmed.ncbi.nlm.nih.gov/31068470/