The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients

Sporadic Creutzfeldt-Jakob disease (sCJD) is the most prevalent of the human prion diseases, which are fatal and transmissible neurodegenerative diseases caused by the infectious prion protein (PrP(Sc)). The origin of sCJD is unknown, although the initiating event is thought to be the stochastic mis...

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Publicat a:PLoS Pathog
Autors principals: Moore, Roger A., Head, Mark W., Ironside, James W., Ritchie, Diane L., Zanusso, Gianluigi, Pyo Choi, Young, Priola, Suzette A.
Format: Artigo
Idioma:Inglês
Publicat: Public Library of Science 2016
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4740439/
https://ncbi.nlm.nih.gov/pubmed/26840342
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.ppat.1005416
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