Neuropathological phenotype and ‘prion protein’ genotype correlation in sporadic Creutzfeldt-Jakob disease
- 1 September 1994
- journal article
- Published by Elsevier in Neuroscience Letters
- Vol. 179 (1-2) , 50-52
- https://doi.org/10.1016/0304-3940(94)90932-6
Abstract
No abstract availableKeywords
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- Fatal Familial Insomnia, a Prion Disease with a Mutation at Codon 178 of the Prion Protein GeneNew England Journal of Medicine, 1992
- CJD discrepancyNature, 1991
- Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob diseaseNature, 1991