1. Genetic variants in SCN5A promoter are associated with arrhythmia phenotype severity in patients with heterozygous loss-of-function mutation;Park;Heart Rhythm,2011
2. Pleiotropic mutations in ion channels: what lies behind them?;Crotti;Heart Rhythm,2011
3. The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome;Makita;J Clin Invest,2008
4. A common HERG polymorphism, K897T, acts as a genetic modifier of the congenital long QT syndrome;Crotti;Circulation,2005
5. Genes and cardiac repolarization: the challenge ahead;Rubart;Circulation,2005