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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...
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| Huvudupphovsmän: | , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Public Library of Science
2013
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| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3700981/ https://ncbi.nlm.nih.gov/pubmed/23843953 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0066352 |
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