High Risk for Bradyarrhythmic Complications in Patients With Brugada Syndrome Caused by SCN5AGene Mutations
- 1 December 2005
- journal article
- case report
- Published by Elsevier in Journal of the American College of Cardiology
- Vol. 46 (11) , 2100-2106
- https://doi.org/10.1016/j.jacc.2005.08.043
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Right bundle branch block, persistent ST segment elevation and sudden cardiac death: A distinct clinical and electrocardiographic syndrome: A multicenter reportPublished by Elsevier ,2010
- Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)Journal of Clinical Investigation, 2003
- The Cardiac Sodium Channel: Gating Function and Molecular PharmacologyJournal of Molecular and Cellular Cardiology, 2001
- The Brugada Syndrome: Ionic Basis and Arrhythmia MechanismsJournal of Cardiovascular Electrophysiology, 2001
- Clinical and Genetic Heterogeneity of Right Bundle Branch Block and ST-Segment Elevation SyndromeCirculation, 2000
- A novel SCN5A mutation associated with idiopathic ventricular fibrillation without typical ECG findings of Brugada syndromeFEBS Letters, 2000
- Cardiac conduction defects associate with mutations in SCN5ANature Genetics, 1999
- Genetic basis and molecular mechanism for idiopathic ventricular fibrillationNature, 1998
- Further Characterization of the Syndrome of Right Bundle Branch Block, ST Segment Elevation, and Sudden Cardiac DeathJournal of Cardiovascular Electrophysiology, 1997
- Molecular mechanism for an inherited cardiac arrhythmiaNature, 1995