Chaperone activity of niflumic acid on ClC-1 chloride channel mutants causing myotonia congenita.
ClC-1 chloride channel
drug repurposing
myotonia congenita
niflumic acid
precision medicine
Journal
Frontiers in pharmacology
ISSN: 1663-9812
Titre abrégé: Front Pharmacol
Pays: Switzerland
ID NLM: 101548923
Informations de publication
Date de publication:
2022
2022
Historique:
received:
31
05
2022
accepted:
08
07
2022
entrez:
29
8
2022
pubmed:
30
8
2022
medline:
30
8
2022
Statut:
epublish
Résumé
Myotonia congenita (MC) is an inherited rare disease characterized by impaired muscle relaxation after contraction, resulting in muscle stiffness. It is caused by loss-of-function mutations in the skeletal muscle chloride channel ClC-1, important for the stabilization of resting membrane potential and for the repolarization phase of action potentials. Thanks to
Identifiants
pubmed: 36034862
doi: 10.3389/fphar.2022.958196
pii: 958196
pmc: PMC9403836
doi:
Types de publication
Journal Article
Langues
eng
Pagination
958196Informations de copyright
Copyright © 2022 Altamura, Conte, Campanale, Laghetti, Saltarella, Camerino, Imbrici and Desaphy.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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