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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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Detalles Bibliográficos
Autores principales:	Barria, Marcelo A, Lee, Andrew, Green, Alison JE, Knight, Richard, Head, Mark W
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2018
Materias:	Brief Definitive Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5903693/ https://www.ncbi.nlm.nih.gov/pubmed/29665324 http://dx.doi.org/10.1002/cjp2.90

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