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Phenotypic diversity in ALS and the role of poly-conformational protein misfolding
In many types of familial amyotrophic lateral sclerosis (fALS), mutations cause proteins to gain toxic properties that mediate neurodegenerative processes. It is becoming increasingly clear that the proteins involved in ALS, and those responsible for a host of other neurodegenerative diseases, share...
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| Publicado no: | Acta Neuropathol |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7956917/ https://ncbi.nlm.nih.gov/pubmed/32930869 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00401-020-02222-x |
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