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Activation and Inactivation of the Voltage-Gated Sodium Channel: Role of Segment S5 Revealed by a Novel Hyperkalaemic Periodic Paralysis Mutation

Hyperkalaemic periodic paralysis, paramyotonia congenita, and potassium-aggravated myotonia are three autosomal dominant skeletal muscle disorders linked to the SCN4A gene encoding the α-subunit of the human voltage-sensitive sodium channel. To date, ∼20 point mutations causing these disorders have...

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Detalhes bibliográficos
Publicado no:J Neurosci
Main Authors: Bendahhou, Saïd, Cummins, Theodore R., Tawil, Rabi, Waxman, Stephen G., Ptácek, Louis J.
Formato: Artigo
Idioma:Inglês
Publicado em: Society for Neuroscience 1999
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6782655/
https://ncbi.nlm.nih.gov/pubmed/10366610
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.19-12-04762.1999
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