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- W1987802048 endingPage "609" @default.
- W1987802048 startingPage "598" @default.
- W1987802048 abstract "The recognition that variant Creutzfeldt–Jakob disease (vCJD) is caused by the same prion strain as bovine spongiform encephalopathy in cattle has dramatically highlighted the need for a precise understanding of the molecular biology of human prion diseases. Detailed clinical, pathological and molecular data from a large number of human prion disease patients indicate that phenotypic diversity in human prion disease relates in part to the propagation of disease-related PrP isoforms with distinct physicochemical properties. Incubation periods of prion infection in humans can exceed 50 years and therefore it will be some years before the extent of any human vCJD epidemic can be predicted with confidence." @default.
- W1987802048 created "2016-06-24" @default.
- W1987802048 creator A5014140779 @default.
- W1987802048 creator A5028812792 @default.
- W1987802048 date "2007-06-01" @default.
- W1987802048 modified "2023-09-30" @default.
- W1987802048 title "Update on human prion disease" @default.
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