Publications
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Filters: Author is Acharfi, Said [Clear All Filters]
, “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, pp. 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, pp. 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, pp. 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, pp. 1513-21, 2003.
, “Expression and intracellular localization of an SCN5A double mutant R1232W/T1620M implicated in Brugada syndrome.”, Circ Res, vol. 90, no. 1, pp. E11-6, 2002.
