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Excitability properties of mouse and human skeletal muscle fibres compared by muscle velocity recovery cycles
Mouse models of skeletal muscle channelopathies are not phenocopies of human disease. In some cases (e.g., Myotonia Congenita) the phenotype is much more severe, whilst in others (e.g. Hypokalaemic periodic paralysis) rodent physiology is protective. This suggests a species’ difference in muscle exc...
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| Pubblicato in: | Neuromuscul Disord |
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| Autori principali: | , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2022
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7614892/ https://ncbi.nlm.nih.gov/pubmed/35339342 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nmd.2022.02.011 |
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