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Article

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

BMJ (Clinical research ed.) - 30 Jan 1993

Collinge J, Palmer M S, Campbell T, Sidle K C, Carroll D, Harding A

Abstract excerpt

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 department. SUBJECTS: Patients suspected to have Creutzfeldt-Jakob disease and other neurodegenerative diseases....

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Identifiers

PMID: 8461647
DOI: 10.1136/bmj.306.6873.301
PMCID: PMC1676853

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Source receipt: pubmed, retrieved 7 Sept 2026.

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