Hypokalaemic periodic paralysis with a charge-retaining substitution in the voltage sensor

Familial hypokalaemic periodic paralysis is a rare skeletal muscle disease caused by the dysregulation of sarcolemmal excitability. Hypokalaemic periodic paralysis is characterized by repeated episodes of paralytic attacks with hypokalaemia, and several variants in CACNA1S coding for Ca(V)1.1 and SC...

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Detalles Bibliográficos
Autores principales: Kubota, Tomoya, Wu, Fenfen, Vicart, Savine, Nakaza, Maki, Sternberg, Damien, Watanabe, Daisuke, Furuta, Mitsuru, Kokunai, Yosuke, Abe, Tatsuya, Kokubun, Norito, Fontaine, Bertrand, Cannon, Stephen C, Takahashi, Masanori P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519726/
https://www.ncbi.nlm.nih.gov/pubmed/33005891
http://dx.doi.org/10.1093/braincomms/fcaa103

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519726/
https://www.ncbi.nlm.nih.gov/pubmed/33005891
http://dx.doi.org/10.1093/braincomms/fcaa103

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