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Article

Prion disease with a 144 base pair insertion: unusual cerebellar prion protein immunoreactivity.

Acta neuropathologica - 1 Nov 2005

Gelpi Ellen, Kovacs Gabor G, Ströbel Thomas, Koperek Oskar, Voigtländer Till, Liberski Pawel P, Budka Herbert

Abstract excerpt

Sporadic, acquired, and genetic human prion diseases are characterized neuropathologically by distinct deposition patterns of the abnormal, disease-associated form of the prion protein (PrP(sc)). In addition to mutations in the prion protein gene (PRNP), PrP(sc) immunostaining patterns correlate with molecular phenotypes of prion diseases defined by the PRNP polymorphism at codon 129 and with protease-resistant...

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Identifiers

PMID: 16155763
DOI: 10.1007/s00401-005-1073-x

Genes

PRNP

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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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