Publications
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Filtres: Author is Acharfi, Said [Enlever les filtres]
, « The C-terminal region as a modulator of rNa(v)1.7 and rNa(v)1.8 expression levels. », FEBS Lett, vol. 559, nᵒ 1-3, p. 39-44, 2004.
, « A novel SCN5A mutation manifests as a malignant form of long QT syndrome with perinatal onset of tachycardia/bradycardia. », Cardiovasc Res, vol. 64, nᵒ 2, p. 268-78, 2004.
, « 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.
, « A novel mutation in SCN5A, delQKP 1507-1509, causing long QT syndrome: role of Q1507 residue in sodium channel inactivation. », J Mol Cell Cardiol, vol. 35, nᵒ 12, p. 1513-21, 2003.
, « Expression and intracellular localization of an SCN5A double mutant R1232W/T1620M implicated in Brugada syndrome. », Circ Res, vol. 90, nᵒ 1, p. E11-6, 2002.
