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Prion Diseases: From Protein to Cell Pathology
Prion diseases or transmissible spongiform encephalopathies are fatal neurodegenerative conditions in humans and animals that originate spontaneously, genetically or by infection. Conformational change of the normal (cellular) form of prion protein (PrP(c)) to a pathological, disease-associated form...
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| Autors principals: | , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society for Investigative Pathology
2008
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2258253/ https://ncbi.nlm.nih.gov/pubmed/18245809 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2353/ajpath.2008.070442 |
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