Publications
Export 7 results:
Filtres: Author is Christé, Georges [Enlever les filtres]
, « Genetic associations of protein-coding variants in human disease. », Nature, vol. 603, nᵒ 7899, p. 95-102, 2022.
, « The variant hERG/R148W associated with LQTS is a mutation that reduces current density on co-expression with the WT. », Gene, vol. 536, nᵒ 2, p. 348-56, 2014.
, « Sodium overload due to a persistent current that attenuates the arrhythmogenic potential of a novel LQT3 mutation. », Front Pharmacol, vol. 4, p. 126, 2013.
, « Sudden death of cardiac origin and psychotropic drugs. », Front Pharmacol, vol. 3, p. 76, 2012.
, « Characterization of novel KCNH2 mutations in type 2 long QT syndrome manifesting as seizures. », Can J Cardiol, vol. 25, nᵒ 8, p. 455-62, 2009.
, « In utero onset of long QT syndrome with atrioventricular block and spontaneous or lidocaine-induced ventricular tachycardia: compound effects of hERG pore region mutation and SCN5A N-terminus variant. », Heart Rhythm, vol. 5, nᵒ 11, p. 1567-74, 2008.
, « A new C-terminal hERG mutation A915fs+47X associated with symptomatic LQT2 and auditory-trigger syncope. », Heart Rhythm, vol. 5, nᵒ 11, p. 1577-86, 2008.
