New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindred-Reference-Cited by-同舟云学术

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New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindred

Published:1991-02 Issue:8738 Volume:337 Page:425
ISSN:0140-6736
Container-title:The Lancet
language:en
Short-container-title:The Lancet

Author:

Goldfarb LevG.,Haltia Matti,Brown Paul,Nieto Ana,Kovanen Jussi,Richard Mccombie W.,Trapp Susan,Carleton Gajdusek D.

Publisher

Elsevier BV

Subject

General Medicine

Reference8 articles.

1. Mutation in codon 200 of scrapie amyloid protein gene in two clusters of Creutzfeldt-Jakob disease in Slovakia;Goldfarb;Lancet,1990

2. Mutation in codon 200 of scrapie amyloid precursor gene linked to Creutzfeldt-Jakob disease in Sephardic Jews of Libyan and non-Libyan origin;Goldfarb;Lancet,1990

3. Descriptive epidemiology of Creutzfeldt-Jakob disease in Finland;Kovanen;Acta Neurol Scand,1988

4. Creutzfeldt-Jakob disease of long duration: clinico-pathological characteristics, transmissibility, and differential diagnosis;Brown;Ann Neurol,1984

5. Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Straussler Scheinker syndrome;Goldgaber;Exp Neurol,1989

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