Cluster of Creutzfeldt–Jakob disease in France associated with the codon 200 mutation (E200K) in the prion protein gene
- 1 July 1998
- journal article
- Published by Wiley in European Journal of Neurology
- Vol. 5 (4) , 375-379
- https://doi.org/10.1046/j.1468-1331.1998.540375.x
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Molecular biology and pathogenesis of prion diseasesTrends in Biochemical Sciences, 1996
- Molecular genetics of prion diseases in FranceNeurology, 1994
- A new point mutation in the prion protein gene at codon 210 in Creutzfeldt‐Jakob diseaseNeurology, 1993
- Inherited prion disease (PrP lysine 200) in Britain: two case reports.BMJ, 1993
- Familial Creutzfeldt-Jakob disease in Chile is associated with the codon 200 mutation of the PRNP amyloid precursor gene on chromosome 20Journal of the Neurological Sciences, 1992
- Creutzfeldt-Jacob disease associated with the PRNP codon 200LYS mutation: An analysis of 45 familiesEuropean Journal of Epidemiology, 1991
- Mutation in codon 200 of scrapie amyloid precursor gene linked to Creutzfeldt-Jakob disease in Sephardic Jews of Libyan and non-Libyan originThe Lancet, 1990
- Mutation in codon 200 of scrapie amyloid protein gene in two clusters of Creutzfeldt-Jakob disease in SlovakiaThe Lancet, 1990
- Identical mutation in unrelated patients with Creutzfeldt-Jakob diseaseThe Lancet, 1990
- Descriptive Epidemiology of Creutzfeldt-Jakob Disease in ChileArchives of Neurology, 1980