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Genetic ablation of complement C3 attenuates muscle pathology in dysferlin-deficient mice
Mutations in the dysferlin gene underlie a group of autosomal recessive muscle-wasting disorders denoted as dysferlinopathies. Dysferlin has been shown to play roles in muscle membrane repair and muscle regeneration, both of which require vesicle-membrane fusion. However, the mechanism by which musc...
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| Główni autorzy: | , , , , , , , , , , |
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| Format: | Artigo |
| Język: | Inglês |
| Wydane: |
American Society for Clinical Investigation
2010
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| Hasła przedmiotowe: | |
| Dostęp online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2993587/ https://ncbi.nlm.nih.gov/pubmed/21060153 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI42390 |
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