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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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| Publicado no: | Neuromuscul Disord |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2022
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| Assuntos: | |
| Acesso em linha: | 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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