Reduced sodium channel function unmasks residual embryonic slow conduction in the adult right ventricular outflow tract.
Boukens, Bas J; Sylva, Marc; de Gier-de Vries, Corrie; Remme, Carol Ann; Bezzina, Connie R; Christoffels, Vincent M; Coronel, Ruben.
; 113(2): 137-41, 2013 Jul 05.
Artigo em Inglês | MEDLINE | ID: mdl-23661717
A novel NaV1.5 voltage sensor mutation associated with severe atrial and ventricular arrhythmias.
Kir2.1 & Na<sub>v</sub>1.5 in Sickness and in Health: Who Needs a Chaperone When They Have an Alpha Partner?
Regulation of Cardiac Voltage-Gated Sodium Channel by Kinases: Roles of Protein Kinases A and C.
A Novel SCN5A Variant Associated with Abnormal Repolarization, Atrial Fibrillation, and Reversible Cardiomyopathy.
Mechanistic links between Na+ channel (SCN5A) mutations and impaired cardiac pacemaking in sick sinus syndrome.
Autonomic modulation of the electrical substrate in mice haploinsufficient for cardiac sodium channels: a model of the Brugada syndrome.
Gene-environment interaction between SCN5A-1103Y and hypokalemia influences QT interval prolongation in African Americans: the Jackson Heart Study.
Cardiac Arrhythmias Related to Sodium Channel Dysfunction.
Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram.
Systematic re-evaluation of SCN5A variants associated with Brugada syndrome.