Associated Papers
Sporadic Erythromelalgia Associated with a Homozygous Carrier of Common Missense Polymorphism in SCN9A Gene Coding for NaV1.7 Voltage-gated Sodium Channel.
Janicki PK et al.
Cureus, 2019
Defective fast inactivation recovery of Nav 1.4 in congenital myasthenic syndrome.
Arnold WD et al.
Annals of Neurology, 2015
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