Publications
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Filtres: Author is Pouliot, Valérie [Enlever les filtres]
, « Novel G1481V and Q1491H SCN5A Mutations Linked to Long QT Syndrome Destabilize the Nav1.5 Inactivation State. », CJC Open, vol. 3, nᵒ 3, p. 256-266, 2021.
, « A204E mutation in Na1.4 DIS3 exerts gain- and loss-of-function effects that lead to periodic paralysis combining hyper- with hypo-kalaemic signs. », Sci Rep, vol. 8, nᵒ 1, p. 16681, 2018.
, « 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.
, « A proton leak current through the cardiac sodium channel is linked to mixed arrhythmia and the dilated cardiomyopathy phenotype. », PLoS One, vol. 7, nᵒ 5, p. e38331, 2012.
, « Biophysical characteristics of a new mutation on the KCNQ1 potassium channel (L251P) causing long QT syndrome. », Can J Physiol Pharmacol, vol. 81, nᵒ 2, p. 129-34, 2003.
