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Article

Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features.

Brain : a journal of neurology - 1 Jun 1992

Collinge J, Brown J, Hardy J, Mullan M, Rossor M N, Baker H, Crow T J, Lofthouse R, Poulter M, Ridley R

Abstract excerpt

A large family with autosomal dominant segregation of presenile dementia, and other neurological and behavioural features is described. At various times, family members have carried diagnoses of Alzheimer's disease, Huntington's disease, Parkinson's disease, myoclonic epilepsy, atypical dementia, Pick's disease, Creutzfeldt-Jakob disease and Gerstmann-Sträussler syndrome. Molecular genetic studies have enabled...

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Identifiers

PMID: 1352725
DOI: 10.1093/brain/115.3.687

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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