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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

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Description scientific article published on 01 August 2011
Author/s

author: Stéphane Haïk  Jean-Jacques Hauw 

Publication date August 1, 2011
Language English
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https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1365-2990.2011.01179.x

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