Publications
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Filters: Author is Ficker, Eckhard [Clear All Filters]
, “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, pp. 348-56, 2014.
, “Characterization of novel KCNH2 mutations in type 2 long QT syndrome manifesting as seizures.”, Can J Cardiol, vol. 25, no. 8, pp. 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, pp. 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, pp. 1577-86, 2008.
