Prion protein mutation in family first reported by Gerstmann, Sträussler, and Scheinker
Author:
Publisher
Elsevier BV
Subject
General Medicine
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1. Gerstmann—Sträussler disease: a familial case with common PRNP mutation and atypical features;Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova;2023
2. Shortening heparan sulfate chains prolongs survival and reduces parenchymal plaques in prion disease caused by mobile, ADAM10-cleaved prions;Acta Neuropathologica;2019-10-31
3. Gerstmann-Sträussler-Scheinker disease: A case report;World Journal of Clinical Cases;2019-02-06
4. Dominantly inherited prion protein cerebral amyloidoses – a modern view of Gerstmann–Sträussler–Scheinker;Human Prion Diseases;2018
5. High phenotypic variability in Gerstmann-Sträussler-Scheinker disease;Arquivos de Neuro-Psiquiatria;2017-06
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