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Review
. 2017 Nov 30;13(11):e1006642.
doi: 10.1371/journal.ppat.1006642. eCollection 2017 Nov.

Public health risks from subclinical variant CJD

Affiliations
Review

Public health risks from subclinical variant CJD

Abigail B Diack et al. PLoS Pathog. .
No abstract available

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Conflict of interest statement

The authors have declared that no competing interests exist.

References

    1. National CJD Research and Surveillance Unit (2017) Creutzfeldt-Jakob disease in the UK. http://www.cjd.ed.ac.uk. Accessed on August 22, 2017.
    1. Bishop MT, Hart P, Aitchison L, Baybutt HN, Plinston C, et al. (2006) Predicting susceptibility and incubation time of human-to-human transmission of vCJD. Lancet Neurol 5: 393–398. doi: 10.1016/S1474-4422(06)70413-6 - DOI - PubMed
    1. Diack AB, Head MW, McCutcheon S, Boyle A, Knight R, et al. (2014) Variant CJD. 18 years of research and surveillance. Prion 8: 286–295. doi: 10.4161/pri.29237 - DOI - PMC - PubMed
    1. Peden AH, Head MW, Ritchie DL, Bell JE, Ironside JW (2004) Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient. Lancet 364: 527–529. doi: 10.1016/S0140-6736(04)16811-6 - DOI - PubMed
    1. Bishop MT, Diack AB, Ritchie DL, Ironside JW, Will RG, et al. (2013) Prion infectivity in the spleen of a PRNP heterozygous individual with subclinical variant Creutzfeldt-Jakob disease. Brain 136: 1139–1145. - PMC - PubMed

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