A Mixed Periodic Paralysis & Myotonia Mutant, P1158S, Imparts pH-Sensitivity in Skeletal Muscle Voltage-gated Sodium Channels

Skeletal muscle channelopathies, many of which are inherited as autosomal dominant mutations, include myotonia and periodic paralysis. Myotonia is defined by a delayed relaxation after muscular contraction, whereas periodic paralysis is defined by episodic attacks of weakness. One sub-type of period...

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Detalles Bibliográficos
Autores principales: Ghovanloo, Mohammad-Reza, Abdelsayed, Mena, Peters, Colin H., Ruben, Peter C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5908869/
https://www.ncbi.nlm.nih.gov/pubmed/29674667
http://dx.doi.org/10.1038/s41598-018-24719-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5908869/
https://www.ncbi.nlm.nih.gov/pubmed/29674667
http://dx.doi.org/10.1038/s41598-018-24719-y

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