Molecular Pathology of Fatal Familial Insomnia

Fatal familial insomnia (FFI) is linked to a mutation at codon 178 of the prion protein gene, coupled with the methionine codon at position 129, the site of a methionine/valine polymorphism. The D178N mutation coupled with the 129 valine codon is linked to a subtype of Creutzfeldt‐Jakob disease (CJD...

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Bibliografiske detaljer
Udgivet i:Brain Pathol
Main Authors: Parchi, Piero, Petersen, Robert B., Chen, Shu G., Autilio‐Gambetti, L., Capellari, Sabina, Monari, Lucia, Cortelli, Pietro, Montagna, Pasquale, Lugaresi, Elio, Gambetti, Pierluigi
Format: Artigo
Sprog:Inglês
Udgivet: Blackwell Publishing Ltd 2006
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Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC8098344/
https://ncbi.nlm.nih.gov/pubmed/9669705
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1750-3639.1998.tb00176.x
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