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The C-terminal region as a modulator of rNa(v)1.7 and rNa(v)1.8 expression levels.
FEBS Lett. 2004 Feb 13;559(1-3):39-44. doi: 10.1016/S0014-5793(04)00019-5.
FEBS Lett. 2004.
PMID: 14960304
Free article.
Expression and intracellular localization of an SCN5A double mutant R1232W/T1620M implicated in Brugada syndrome.
Baroudi G, Acharfi S, Larouche C, Chahine M.
Baroudi G, et al. Among authors: acharfi s.
Circ Res. 2002 Jan 11;90(1):E11-6.
Circ Res. 2002.
PMID: 11786529
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Biophysical characteristics of a new mutation on the KCNQ1 potassium channel (L251P) causing long QT syndrome.
Deschênes D, Acharfi S, Pouliot V, Hegele R, Krahn A, Daleau P, Chahine M.
Deschênes D, et al. Among authors: acharfi s.
Can J Physiol Pharmacol. 2003 Feb;81(2):129-34. doi: 10.1139/y02-162.
Can J Physiol Pharmacol. 2003.
PMID: 12710526
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A novel mutation in SCN5A, delQKP 1507-1509, causing long QT syndrome: role of Q1507 residue in sodium channel inactivation.
Keller DI, Acharfi S, Delacrétaz E, Benammar N, Rotter M, Pfammatter JP, Fressart V, Guicheney P, Chahine M.
Keller DI, et al. Among authors: acharfi s.
J Mol Cell Cardiol. 2003 Dec;35(12):1513-21. doi: 10.1016/j.yjmcc.2003.08.007.
J Mol Cell Cardiol. 2003.
PMID: 14654377
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A novel SCN5A mutation manifests as a malignant form of long QT syndrome with perinatal onset of tachycardia/bradycardia.
Chang CC, Acharfi S, Wu MH, Chiang FT, Wang JK, Sung TC, Chahine M.
Chang CC, et al. Among authors: acharfi s.
Cardiovasc Res. 2004 Nov 1;64(2):268-78. doi: 10.1016/j.cardiores.2004.07.007.
Cardiovasc Res. 2004.
PMID: 15485686
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