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From Prion Diseases to Prion-Like Propagation Mechanisms of Neurodegenerative Diseases
Prion diseases are fatal neurodegenerative sporadic, inherited, or acquired disorders. In humans, Creutzfeldt-Jakob disease is the most studied prion disease. In animals, the most frequent prion diseases are scrapie in sheep and goat, bovine spongiform encephalopathy in cattle, and the emerging chro...
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| Autors principals: | , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Hindawi Publishing Corporation
2013
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3810426/ https://ncbi.nlm.nih.gov/pubmed/24222767 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2013/975832 |
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