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Features of wild-type human SOD1 limit interactions with misfolded aggregates of mouse G86R Sod1
Mutations in the gene encoding superoxide dismutase 1 (SOD1) account for about 20% of the cases of familial amyotrophic lateral sclerosis (fALS). It is well established that mutations in SOD1, associated with fALS, heighten the propensity of the protein to misfold and aggregate. Although aggregation...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3881023/ https://ncbi.nlm.nih.gov/pubmed/24341866 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1326-8-46 |
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