Polymorphisms of the prion protein gene in Italian patients with Creutzfeldt-Jakob disease
- 1 October 1994
- journal article
- Published by Springer Nature in Human Genetics
- Vol. 94 (4) , 375-379
- https://doi.org/10.1007/bf00201596
Abstract
No abstract availableKeywords
This publication has 40 references indexed in Scilit:
- Similar genetic susceptibility in iatrogenic and sporadic Creutzfeldt-Jakob diseaseJournal of General Virology, 1994
- A new point mutation of the prion protein gene in Creutzfeldt‐Jakob diseaseAnnals of Neurology, 1993
- Human Pituitary Growth Hormone and Creutzfeldt-Jakob DiseaseHormone Research, 1993
- Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tanglesNature Genetics, 1992
- Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein geneNature Genetics, 1992
- Aminoacid polymorphism in human prion protein and age at death in inherited prion diseaseThe Lancet, 1991
- New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindredThe Lancet, 1991
- 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
- Linkage of a prion protein missense variant to Gerstmann–Sträussler syndromeNature, 1989