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Changes in Resurgent Sodium Current Contribute to the Hyperexcitability of Muscles in Patients with Paramyotonia Congenita
Paramyotonia congenita (PMC) is a rare hereditary skeletal muscle disorder. The major symptom, muscle stiffness, is frequently induced by cold exposure and repetitive exercise. Mutations in human SCN4A gene, which encodes the α-subunit of Na(v)1.4 channel, are responsible for PMC. Mutation screening...
Autores principales: | Huang, Chiung-Wei, Lai, Hsing-Jung, Lin, Pi-Chen, Lee, Ming-Jen |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7826575/ https://www.ncbi.nlm.nih.gov/pubmed/33430134 http://dx.doi.org/10.3390/biomedicines9010051 |
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