ClC-1 Chloride Channel: Inputs on the Structure–Function Relationship of Myotonia Congenita-Causing Mutations

Myotonia congenita is a hereditary muscle disease mainly characterized by muscle hyperexcitability, which leads to a sustained burst of discharges that correlates with the magnitude and duration of involuntary aftercontractions, muscle stiffness, and hypertrophy. Mutations in the chloride voltage-ga...

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Detalles Bibliográficos
Autores principales: Brenes, Oscar, Pusch, Michael, Morales, Fernando
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10604815/
https://www.ncbi.nlm.nih.gov/pubmed/37892996
http://dx.doi.org/10.3390/biomedicines11102622

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10604815/
https://www.ncbi.nlm.nih.gov/pubmed/37892996
http://dx.doi.org/10.3390/biomedicines11102622

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