Autophagy is affected in patients with hypokalemic periodic paralysis: an involvement in vacuolar myopathy?

Hypokalemic periodic paralysis is an autosomal dominant, rare disorder caused by variants in the genes for voltage-gated calcium channel Ca(V)1.1 (CACNA1S) and Na(V)1.4 (SCN4A). Patients with hypokalemic periodic paralysis may suffer from periodic paralysis alone, periodic paralysis co-existing with...

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Detalles Bibliográficos
Autores principales: Krag, Thomas O., Holm-Yildiz, Sonja, Witting, Nanna, Vissing, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8201813/
https://www.ncbi.nlm.nih.gov/pubmed/34120654
http://dx.doi.org/10.1186/s40478-021-01212-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8201813/
https://www.ncbi.nlm.nih.gov/pubmed/34120654
http://dx.doi.org/10.1186/s40478-021-01212-8

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