The mechanism underlying transient weakness in myotonia congenita

In addition to the hallmark muscle stiffness, patients with recessive myotonia congenita (Becker disease) experience debilitating bouts of transient weakness that remain poorly understood despite years of study. We performed intracellular recordings from muscle of both genetic and pharmacologic mous...

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Detalles Bibliográficos
Autores principales: Myers, Jessica H, Denman, Kirsten, DuPont, Chris, Hawash, Ahmed A, Novak, Kevin R, Koesters, Andrew, Grabner, Manfred, Dayal, Anamika, Voss, Andrew A, Rich, Mark M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8079152/
https://www.ncbi.nlm.nih.gov/pubmed/33904400
http://dx.doi.org/10.7554/eLife.65691

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8079152/
https://www.ncbi.nlm.nih.gov/pubmed/33904400
http://dx.doi.org/10.7554/eLife.65691

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