Regional heterogeneity of cellular prion protein isoforms in the mouse brain

Prion diseases are a group of invariably fatal neurodegenerative disorders that include Creutzfeldt–Jakob disease in humans, scrapie in sheep and goats, and bovine spongiform encephalopathy in cattle. The infectious agent or prion is largely composed of an abnormal isoform (PrPSc) of a host encoded...

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Bibliographic Details
Main Authors: Beringue, V, Mallinson, G, Kaisar, M, Tayebi, M, Sattar, Z, Jackson, G, Anstee, D, Collinge, J, Hawke, S
Format: Journal article
Language:English
Published: Oxford University Press 2003