Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism.

Fatal familial insomnia and a subtype of Creutzfeldt-Jakob disease, two clinically and pathologically distinct diseases, are linked to the same mutation at codon 178 (Asp-178-->Asn) but segregate with different genotypes determined by this mutation and the methionine-valine polymorphism at codon 129...

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Veröffentlicht in:	Proc Natl Acad Sci U S A
Hauptverfasser:	Monari, L, Chen, S G, Brown, P, Parchi, P, Petersen, R B, Mikol, J, Gray, F, Cortelli, P, Montagna, P, Ghetti, B
Format:	Artigo
Sprache:	Inglês
Veröffentlicht:	National Academy of Sciences 1994
Schlagworte:	Research Article
Online-Zugang:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC43466/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7908444/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.91.7.2839
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