Codon 200 mutation in a new family of Chilean origin with Creutzfeldt-Jakob disease.
Open Access
- 1 July 1996
- journal article
- research article
- Published by BMJ in Journal of Neurology, Neurosurgery & Psychiatry
- Vol. 61 (1) , 111-112
- https://doi.org/10.1136/jnnp.61.1.111
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Small virus-like structure in brains from cases of sporadic and familial Creutzfeldt-Jakob diseaseThe Lancet, 1994
- Japanese family with Creutzfeldt‐Jakob disease with codon 200 point mutation of the prion protein geneNeurology, 1994
- Mutation and polymorphism of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease (CJD).1993
- Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation.Journal of Neurology, Neurosurgery & Psychiatry, 1993
- Creutzfeldt-Jacob disease associated with the PRNP codon 200LYS mutation: An analysis of 45 familiesEuropean Journal of Epidemiology, 1991