B. Fontaine, E. Fournier, D. Sternberg, S. Vicart, and N. Tabti, Hypokalemic periodic paralysis: A model for a clinical and research approach to a rare disorder, Neurotherapeutics, vol.84, issue.2, pp.225-257, 2007.
DOI : 10.1016/j.nurt.2007.01.002

T. Miller, M. Dias-da-silva, H. Miller, H. Kwiecinski, J. Mendell et al., Correlating phenotype and genotype in the periodic paralyses, Neurology, vol.63, issue.9, pp.1647-55, 2004.
DOI : 10.1212/01.WNL.0000143383.91137.00

D. Sternberg, T. Maisonobe, K. Jurkat-rott, S. Nicole, E. Launay et al., Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A, Brain, vol.124, issue.6, pp.1091-1100, 2001.
DOI : 10.1093/brain/124.6.1091

R. Horn, Coupled Movements in Voltage-gated Ion Channels, The Journal of General Physiology, vol.73, issue.4, pp.449-53, 2002.
DOI : 10.1017/S0033583598003448

C. Gandhi and E. Isacoff, Molecular Models of Voltage Sensing, The Journal of General Physiology, vol.74, issue.4, pp.455-63, 2002.
DOI : 10.1017/S0033583598003448

P. Lapie, C. Goudet, J. Nargeot, B. Fontaine, and L. P. , subunit as expressed in mouse L cells, FEBS Letters, vol.7, issue.3, pp.244-252, 1996.
DOI : 10.1016/0014-5793(96)00173-1

J. Morrill, R. Brown, . Jr, and S. Cannon, Gating of the L-type Ca channel in human skeletal myotubes: an activation defect caused by the hypokalemic periodic paralysis mutation R528H, J Neurosci, vol.18, pp.10320-10354, 1998.

I. Sipos, K. Jurkat-rott, C. Harasztosi, B. Fontaine, L. Kovacs et al., Skeletal muscle DHP receptor mutations alter calcium currents in human hypokalaemic periodic paralysis myotubes., The Journal of Physiology, vol.483, issue.2, pp.299-306, 1995.
DOI : 10.1113/jphysiol.1995.sp020586

K. Jurkat-rott, N. Mitrovic, C. Hang, A. Kpiuzmekine, P. Iaizzo et al., Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current, Proceedings of the National Academy of Sciences, vol.97, issue.17, pp.9549-54, 2000.
DOI : 10.1073/pnas.97.17.9549

S. Sokolov, T. Scheuer, and W. Catterall, Gating pore current in an inherited ion channelopathy, Nature, vol.53, issue.7131, pp.76-84, 2007.
DOI : 10.1038/nature05598