Uncommon phenotype for a codon 178 mutation of the human PrP gene
- 1 March 1992
- journal article
- letter
- Published by Wiley in Annals of Neurology
- Vol. 31 (3) , 345
- https://doi.org/10.1002/ana.410310321
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
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- The new biology of spongiform encephalopathy: infectious amyloidoses with a genetic twistThe Lancet, 1991
- Codon 178 mutation in ethnically diverse Creutzfeldt-Jakob disease familiesThe Lancet, 1991
- New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindredThe Lancet, 1991
- Familial Creutzfeldt-Jakob diseaseJournal of the Neurological Sciences, 1980