Mutation in codon 200 of scrapie amyloid precursor gene linked to Creutzfeldt-Jakob disease in Sephardic Jews of Libyan and non-Libyan origin
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference10 articles.
1. Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Straussler syndrome;Goldgaber;Exp Neurol,1989
2. Creutzfeldt-Jakob disease and kuru patients lack a mutation consistently found in Gerstmann-Straussler-Scheinker syndrome;Goldfarb;Exp Neurol,1990
3. An identical mutation in unrelated patients with Creutzfeldt-Jakob disease;Goldfarb;Lancet,1990
4. High incidence of Creutzfeldt-Jakob disease in North African immigrants to France;Cathala;Neurology,1985
5. Analytical epidemiology and risk factors of CJD;Mitrová,1990
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