Ventricular fibrillation in Graves disease reveals a rare SCN5A mutation with W1191X variant associated with Brugada syndrome
Stawiarski K, Clarke JD, Pollack A, Winslow R, Majumdar S. Ventricular fibrillation in Graves disease reveals a rare SCN5A mutation with W1191X variant associated with Brugada syndrome. HeartRhythm Case Reports 2020, 7: 95-99. PMID: 33665110, PMCID: PMC7897746, DOI: 10.1016/j.hrcr.2020.11.010.Peer-Reviewed Case Reports and Technical Notes