Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes.Yang P, Kanki H, Drolet B, Yang T, Wei J, Viswanathan PC, Hohnloser SH, Shimizu W, Schwartz PJ, Stanton M, Murray KT, Norris K, George AL, Roden DM
(2002)
Circulation 105: 1943-8
MeSH Terms: Alleles, Animals, Anti-Arrhythmia Agents, CHO Cells, Cation Transport Proteins, Cell Line, Cricetinae, DNA-Binding Proteins, ERG1 Potassium Channel, Electric Conductivity, Ether-A-Go-Go Potassium Channels, Female, Gene Frequency, Genetic Predisposition to Disease, Genetic Variation, Humans, KCNQ Potassium Channels, KCNQ1 Potassium Channel, Long QT Syndrome, Male, Mutation, NAV1.5 Voltage-Gated Sodium Channel, Polymorphism, Genetic, Potassium Channels, Potassium Channels, Voltage-Gated, Sodium Channels, Torsades de Pointes, Trans-Activators, Transcriptional Regulator ERGAdded January 20, 2015