Publications
Export 4 results:
Filtres: Author is Ficker, Eckhard [Enlever les filtres]
, « 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.
, « 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.
