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25. Quantification of surviving cerebellar granule neurones and abnormal prion protein (PrPSc) deposition in sporadic Creutzfeldt-Jakob disease supports a pathogenic role for small PrPSc deposits common to the various molecular subtypes. Faucheux BA; Morain E; Diouron V; Brandel JP; Salomon D; Sazdovitch V; Privat N; Laplanche JL; Hauw JJ; Haïk S Neuropathol Appl Neurobiol; 2011 Aug; 37(5):500-12. PubMed ID: 21450052 [TBL] [Abstract][Full Text] [Related]
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