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Inherited prion disease (PrP lysine 200) in Britain: two case reports.

OBJECTIVE--To identify cases of inherited prion diseases in Britain and to assess their phenotypic features. DESIGN--Screening study of patients suspected clinically to have Creutzfeldt-Jakob disease and other neurodegenerative diseases by prion protein gene analysis. SETTING--Biochemical research d...

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Detalhes bibliográficos
Main Authors: Collinge, J, Palmer, M S, Campbell, T, Sidle, K C, Carroll, D, Harding, A
Formato: Artigo
Idioma:Inglês
Publicado em: 1993
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1676853/
https://ncbi.nlm.nih.gov/pubmed/8461647
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