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Detection of prions in blood from patients with variant Creutzfeldt-Jakob disease
Human prion diseases are infectious and invariably fatal neurodegenerative diseases. They include sporadic Creutzfeldt-Jakob disease (sCJD), the most common form, and variant CJD (vCJD), which is caused by interspecies transmission of prions from cattle infected by bovine spongiform encephalopathy....
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| Publicat a: | Sci Transl Med |
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| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5538786/ https://ncbi.nlm.nih.gov/pubmed/28003548 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1126/scitranslmed.aaf6188 |
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