Rapid amplification of prions from variant Creutzfeldt-Jakob disease cerebrospinal fluid
Author:
Affiliation:
1. National CJD Research & Surveillance Unit, Centre for Clinical Brain Sciences, Deanery of Clinical Medicine; The University of Edinburgh; Edinburgh UK
Funder
Department of Health Policy Research Programme and the Scottish Government
Publisher
Wiley
Subject
Pathology and Forensic Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/cjp2.90/fullpdf
Reference21 articles.
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2. Review: Creutzfeldt-Jakob disease: prion protein type, disease phenotype and agent strain;Head;Neuropathol Appl Neurobiol,2012
3. A new variant of Creutzfeldt-Jakob disease in the UK;Will;Lancet,1996
4. Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale survey;Gill;BMJ,2013
5. Molecular barriers to zoonotic transmission of prions;Barria;Emerg Infect Dis,2014
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