An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing
Top Cited Papers
- 31 January 2010
- journal article
- research article
- Published by Elsevier BV in Heart Rhythm
- Vol. 7 (1), 33-46
- https://doi.org/10.1016/j.hrthm.2009.09.069
Abstract
No abstract availableKeywords
This publication has 38 references indexed in Scilit:
- Genetic Testing for Long-QT SyndromeCirculation, 2009
- Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION® long QT syndrome genetic testHeart Rhythm, 2009
- A Mutation in the β3 Subunit of the Cardiac Sodium Channel Associated With Brugada ECG PhenotypeCirculation: Cardiovascular Genetics, 2009
- SCN5A channelopathies – An update on mutations and mechanismsProgress in Biophysics and Molecular Biology, 2008
- Functional Effects of KCNE3 Mutation and Its Role in the Development of Brugada SyndromeCirculation: Arrhythmia and Electrophysiology, 2008
- Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humansJCI Insight, 2008
- The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndromeJCI Insight, 2008
- Mutation in Glycerol-3-Phosphate Dehydrogenase 1–Like Gene ( GPD1-L ) Decreases Cardiac Na + Current and Causes Inherited ArrhythmiasCirculation, 2007
- Genetic basis of Brugada syndromeHeart Rhythm, 2007
- Nomenclature for the description of human sequence variationsHuman Genetics, 2001