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Re-Assessment of PrP(Sc) Distribution in Sporadic and Variant CJD
Human prion diseases are fatal neurodegenerative disorders associated with an accumulation of PrP(Sc) in the central nervous system (CNS). Of the human prion diseases, sporadic Creutzfeldt-Jakob disease (sCJD), which has no known origin, is the most common form while variant CJD (vCJD) is an acquire...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Public Library of Science
2013
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3700981/ https://www.ncbi.nlm.nih.gov/pubmed/23843953 http://dx.doi.org/10.1371/journal.pone.0066352 |