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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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發表在:Neuromuscul Disord
Main Authors: Suetterlin, K. J., Männikkö, R., Matthews, E., Greensmith, L., Hanna, M.G., Bostock, H., Tan, S.V.
格式: Artigo
語言:Inglês
出版: 2022
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在線閱讀: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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