Q-T Peak Dispersion in Congenital Long QT Syndrome: Possible Marker of Mutation of HERG - Inoue, Masaru; Kiyama, Masaru; Ino, Hidekazu; Shimizu, Masami; Hayashi, Tatsumi; Sakata, Kenji; Terai, Hidenobu; Yamaguchi, Masato; Mabuchi, Hiroshi; Hayashi, Kenshi (Circulation Journal, 2003)
Keywords: Adult; Amino Acid Substitution; Biological and medical sciences; Cardiac dysrhythmias; Cardiology. Vascular system; Cation Transport Proteins; DNA-Binding Proteins; Electrocardiography; ERG1 Potassium Channel; Ether-A-Go-Go Potassium Channels; Female; Heart; Humans; KCNQ Potassium Channels; KCNQ1 Potassium Channel; Long QT syndrome; Long QT Syndrome - classification; Long QT Syndrome - congenital; Long QT Syndrome - genetics; Long QT Syndrome - physiopathology; Male; Medical sciences; Middle Aged; Mutation, Missense; Notched T wave; Potassium Channels - deficiency; Potassium Channels - genetics; Potassium Channels - physiology; Potassium Channels, Voltage-Gated; QT dispersion; Trans-Activators; Transcriptional Regulator ERG; Human; QT interval; Arrhythmia; Potassium ion; Prolonged QT interval; Cardiovascular disease; Ionic channel; Conduction disorder; Genetic determinism; QT dispersion; HERG; Gene; Heart block; Heart disease; Sodium ion; Long QT syndrome; Notched T wave; Mutation