Associated Papers
The Domain II S4-S5 Linker in Nav1.9: A Missense Mutation Enhances Activation, Impairs Fast Inactivation, and Produces Human Painful Neuropathy.
Han C et al.
Neuromolecular Medicine, 2015
Erythromelalgia: a hereditary pain syndrome enters the molecular era.
Waxman SG et al.
Annals of Neurology, 2005
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