Sporadic human prion diseases: molecular insights and diagnosis
Sporadic human prion diseases: molecular insights and diagnosis
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Publisher
England: Elsevier Ltd
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Language
English
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England: Elsevier Ltd
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Summary Human prion diseases can be sporadic, inherited, or acquired by infection. Distinct clinical and pathological characteristics separate sporadic diseases into three phenotypes: Creutzfeldt-Jakob disease (CJD), fatal insomnia, and variably protease-sensitive prionopathy. CJD accounts for more than 90% of all cases of sporadic prion disease; i...
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Sporadic human prion diseases: molecular insights and diagnosis
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TN_cdi_proquest_miscellaneous_1034828132
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1034828132
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ISSN
1474-4422
E-ISSN
1474-4465
DOI
10.1016/S1474-4422(12)70063-7
