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• W2028875969 abstract "A case of sporadic Creutzfeldt-Jakob disease (sCJD) is described in a young Dutch protein prion gene (PRNP) codon 129 valine homozygote. Certain clinical and molecular features of this case overlap those of variant CJD. The case highlights possible difficulties in the differential diagnosis of vCJD and the more rare sCJD subtypes based on molecular features alone." @default.
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• W2028875969 date "2001-01-01" @default.
• W2028875969 modified "2023-09-25" @default.
• W2028875969 title "Sporadic Creutzfeldt-Jakob disease in a young Dutch valine homozygote: Atypical molecular phenotype" @default.
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• W2028875969 doi "https://doi.org/10.1002/ana.1100" @default.
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