Rapid, sensitive and inexpensive detection of SCN5A genetic variations by high resolution melting analysis
- 30 April 2009
- journal article
- Published by Elsevier BV in Clinical Biochemistry
- Vol. 42 (6), 491-499
- https://doi.org/10.1016/j.clinbiochem.2008.10.014
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Cardiac Sodium Channel Overlap Syndromes: Different Faces of SCN5A MutationsTrends in Cardiovascular Medicine, 2008
- Divergent Biophysical Defects Caused by Mutant Sodium Channels in Dilated Cardiomyopathy With ArrhythmiaCirculation Research, 2008
- Cardiac sodium channel mutation in atrial fibrillationHeart Rhythm, 2008
- Dilated cardiomyopathy is associated with reduced expression of the cardiac sodium channel Scn5aCardiovascular Research, 2007
- SCN5A–linked disease syndromes: complex monogenic disorders of cardiac rhythmFuture Cardiology, 2005
- Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutationJCI Insight, 2002
- Clinical, Genetic, and Biophysical Characterization of SCN5A Mutations Associated With Atrioventricular Conduction BlockCirculation, 2002
- A Single Na + Channel Mutation Causing Both Long-QT and Brugada SyndromesCirculation Research, 1999
- Cardiac conduction defects associate with mutations in SCN5ANature Genetics, 1999
- Genetic basis and molecular mechanism for idiopathic ventricular fibrillationNature, 1998