Pathological progression of genetic Creutzfeldt–Jakob disease with a PrP V180I mutation

In comparison to sporadic Creutzfeldt–Jakob disease (sCJD) with MM1-type and MM2- cortical (MM2C)-type, genetic CJD with a prion protein gene V180I mutation (V180I gCJD) is clinically characterized by onset at an older age, slower progress, and the absence of visual disturbances or cerebellar sympto...

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Bibliografiske detaljer
Udgivet i:Prion
Main Authors: Akagi, Akio, Iwasaki, Yasushi, Mimuro, Maya, Kitamoto, Tetsuyuki, Yamada, Masahito, Yoshida, Mari
Format: Artigo
Sprog:Inglês
Udgivet: Taylor & Francis 2018
Fag:
Research Paper
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5871029/
https://ncbi.nlm.nih.gov/pubmed/29264994
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/19336896.2017.1414130
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