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PRNP E146G mutation inherited prion disease: distinctive clinical, pathological and fluid biomarker features. (2025)

First Author: Coysh T

Attributed to: UKDP: Integrated DEmentiA research environment (IDEA) funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1007/s00415-025-13022-2

PubMed Identifier: 40156621

Publication URI: http://europepmc.org/abstract/MED/40156621

Type: Journal Article/Review

Volume: 272

Parent Publication: Journal of neurology

Issue: 4

ISSN: 0340-5354