ArticleResearch square2026
Distinctive properties of the prion protein in the brain and retina in the amyloidosis associated with the PRNP F198S Mutation.
Article in Research square, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Funding
Abstract
Prion protein (PrP) deposits in the form of diffuse and cored plaques occur in most gray matter areas of the brain of individuals affected by Gerstmann-Strässler-Scheinker disease (GSS) associated with the F198S mutation in
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