Ventricular fibrillation in Graves disease reveals a rare SCN5A mutation with W1191X variant associated with Brugada syndrome

HeartRhythm Case Rep. 2020 Nov 20;7(2):95-99. doi: 10.1016/j.hrcr.2020.11.010. eCollection 2021 Feb.
No abstract available

Keywords: Arrhythmias; Brugada syndrome; Genetic mutation; Hyperthyroidism; Implantable cardioverter-defibrillator; Ventricular fibrillation.

Publication types

  • Case Reports