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

Internet

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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