Creutzfeldt-Jakob disease and kuru patients lack a mutation consistently found in the Gerstmann-Sträussler-Scheinker syndrome
- 1 June 1990
- journal article
- research article
- Published by Elsevier in Experimental Neurology
- Vol. 108 (3), 247-250
- https://doi.org/10.1016/0014-4886(90)90130-k
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndromeExperimental Neurology, 1989
- Linkage of a prion protein missense variant to Gerstmann–Sträussler syndromeNature, 1989
- Report of the committee on the genetic constitution of chromosomes 20 and 21Cytogenetic and Genome Research, 1989
- Fibrils from brains of cows with new cattle disease contain scrapie-associated proteinNature, 1988
- A cellular gene encodes scrapie PrP 27-30 proteinCell, 1985
- Novel Proteinaceous Infectious Particles Cause ScrapieScience, 1982
- Morbus Gerstmann-Sträussler-ScheinkerArchiv Fur Psychiatrie Und Nervenkrankheiten, 1981
- Subakute spongiforme Encephalopathie mit multiformer PlaquebildungActa Neuropathologica, 1980
- Unconventional Viruses and the Origin and Disappearance of KuruScience, 1977
- Experimental Transmission of a Kuru-like Syndrome to ChimpanzeesNature, 1966