Identical mutation in unrelated patients with Creutzfeldt-Jakob disease
- 21 July 1990
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 336 (8708), 174-175
- https://doi.org/10.1016/0140-6736(90)91693-5
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Creutzfeldt-Jakob disease and kuru patients lack a mutation consistently found in the Gerstmann-Sträussler-Scheinker syndromeExperimental Neurology, 1990
- Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndromeExperimental Neurology, 1989
- Pro→Leu change at position 102 of prinon protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndromeBiochemical and Biophysical Research Communications, 1989
- DIAGNOSIS OF GERSTMANN-STRÄUSSLER SYNDROME IN FAMILIAL DEMENTIA WITH PRION PROTEIN GENE ANALYSISThe Lancet, 1989
- Linkage of the gene for the scrapie-associated fibril protein (PrP) to the Sip gene in Cheviot sheepVeterinary Record, 1989
- Linkage of a prion protein missense variant to Gerstmann–Sträussler syndromeNature, 1989
- INSERTION IN PRION PROTEIN GENE IN FAMILIAL CREUTZFELDT-IAKOB DISEASEThe Lancet, 1989
- Linkage of prion protein and scrapie incubation time genesCell, 1986