Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob disease
Authors:
- A AlperovitchAAA Alperovitch
- I ZerrIZI Zerr
- M PocchiariMPM Pocchiari
- E MitrovaEME Mitrova
- J de Pedro CuestaJCJ de Pedro Cuesta
- I HegyiIHI Hegyi
- S CollinsSCS Collins
- H KretzschmarHKH Kretzschmar
- C van DujinCDC van Dujin
- Rg WillRWRg Will
- 1 May 1999
- journal article
- Published by Elsevier in The Lancet
- Vol. 353 (9165) , 1673-1674
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Methionine homozygosity at prion gene codon 129 may predispose to sporadic inclusion-body myositisThe Lancet, 1999
- Descriptive epidemiology of Creutzfeldt‐Jakob disease in six european countries, 1993–1995Annals of Neurology, 1998
- Molecular basis of phenotypic variability in sporadc creudeldt‐jakob diseaseAnnals of Neurology, 1996
- Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob diseaseNature, 1991
- Genetic predisposition to iatrogenic Creutzfeldt-Jakob diseaseThe Lancet, 1991