Atypical Prion Protein Conformation in Familial Prion Disease with PRNP P105T Mutation

Protease‐resistant prion protein (PrP(Sc)) is diagnostic of prion disease, yet its detection is frequently difficult. Here, we describe a patient with a PRNP P105T mutation and typical familial prion disease. Brain PrP(Sc) was undetectable by conventional Western blotting and barely detectable after...

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Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Brain Pathol
Päätekijät: Polymenidou, Magdalini, Prokop, Stefan, Jung, Hans H., Hewer, Ekkehard, Peretz, David, Moos, Rita, Tolnay, Markus, Aguzzi, Adriano
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Blackwell Publishing Ltd 2010
Aiheet:
Research Articles
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC8094255/
https://ncbi.nlm.nih.gov/pubmed/20875062
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1750-3639.2010.00439.x
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