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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...
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| Publicat a: | Biomedicines |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
MDPI
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7826575/ https://ncbi.nlm.nih.gov/pubmed/33430134 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/biomedicines9010051 |
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