QuickView for SCN5A;jsessionid=4DED462CD642FBF7C0D0746DA95E64EE (gene)

1. SCN5A channelopathy: arrhythmia, cardiomyopathy, epilepsy and beyond.
2. GPD1L-A306del modifies sodium current in a family carrying the dysfunctional SCN5A-G1661R mutation a…
3. The SCN5A Gene Is a Predictor of Phenotype Severity in Brugada Syndrome: A Comprehensive Literature …
4. Beneficial effects of chronic mexiletine treatment in a human model of SCN5A overlap syndrome.
5. Challenges in Brugada Syndrome Stratification: Investigating SCN5A Mutation Localization and Clinica…

There were no clinical trials for SCN5A;jsessionid=4DED462CD642FBF7C0D0746DA95E64EE