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Rapid amplification of prions from variant Creutzfeldt–Jakob disease cerebrospinal fluid
Human prion diseases constitute a group of infectious and invariably fatal neurodegenerative disorders associated with misfolding of the prion protein. Variant Creutzfeldt–Jakob disease (vCJD) is a zoonotic prion disease linked to oral exposure to the infectious agent that causes bovine spongiform e...
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| Publicado no: | J Pathol Clin Res |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5903693/ https://ncbi.nlm.nih.gov/pubmed/29665324 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/cjp2.90 |
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