Associated Papers
Human skeletal muscle sodium channelopathies.
Vicart S et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2005
Tryptophan substitution of a putative D4S6 gating hinge alters slow inactivation in cardiac sodium channels.
Wang SY et al.
Biophysical Journal, 2005
Genetic disorders of neuromuscular ion channels.
Kleopa KA et al.
Muscle & Nerve, 2002
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