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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Vydáno v:PLoS Pathog
Hlavní autoři: Moore, Roger A., Head, Mark W., Ironside, James W., Ritchie, Diane L., Zanusso, Gianluigi, Pyo Choi, Young, Priola, Suzette A.
Médium: Artigo
Jazyk:Inglês
Vydáno: Public Library of Science 2016
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Research Article
On-line přístup: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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