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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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| Pubblicato in: | Biomedicines |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
MDPI
2021
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| Soggetti: | |
| Accesso online: | 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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