作者: Elizabeth A. Schroder , Don E. Burgess , Cody L. Manning , Yihua Zhao , Arthur J. Moss
DOI: 10.1152/AJPHEART.00341.2014
关键词: Basal (phylogenetics) 、 Phenotype 、 Heart rate 、 QT interval 、 Long QT syndrome 、 Endocrinology 、 Long QT syndrome type 3 、 Biology 、 Internal medicine 、 Circadian rhythm
摘要: Long QT syndrome type 3 (LQT3) is caused by mutations in the SCN5A-encoded Nav1.5 channel. LQT3 patients exhibit time of day-associated abnormal increases their heart rate-corrected (QTc) int...