Iatrogenic and sporadic Creutzfeldt-Jakob disease in 2 sisters without mutation in the prion protein gene

Human genetic prion diseases have invariably been linked to alterations of the prion protein (PrP) gene PRNP. Two sisters died from probable Creutzfeldt-Jakob disease (CJD) in Switzerland within 14 y. At autopsy, both patients had typical spongiform change in their brains accompanied by punctuate de...

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Sparad:
Bibliografiska uppgifter
I publikationen:Prion
Huvudupphovsmän: Frontzek, Karl, Moos, Rita, Schaper, Elke, Jann, Lukas, Herfs, Gregor, Zimmermann, Dieter R, Aguzzi, Adriano, Budka, Herbert
Materialtyp: Artigo
Språk:Inglês
Publicerad: Taylor & Francis 2015
Ämnen:
Short Communications
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC4964856/
https://ncbi.nlm.nih.gov/pubmed/26634863
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/19336896.2015.1121356
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