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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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Detalhes bibliográficos
Main Authors: Rubenstein, Richard, Chang, Binggong
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2013
Assuntos:
Acesso em linha: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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