Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP.

Deposition of PrP amyloid in cerebral vessels in conjunction with neurofibrillary lesions is the neuropathologic hallmark of the dementia associated with a stop mutation at codon 145 of PRNP, the gene encoding the prion protein (PrP). In this disorder, the vascular amyloid in tissue sections and the...

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Vydáno v:	Proc Natl Acad Sci U S A
Hlavní autoři:	Ghetti, B, Piccardo, P, Spillantini, M G, Ichimiya, Y, Porro, M, Perini, F, Kitamoto, T, Tateishi, J, Seiler, C, Frangione, B, Bugiani, O, Giaccone, G, Prelli, F, Goedert, M, Dlouhy, S R, Tagliavini, F
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	National Academy of Sciences 1996
Témata:	Research Article
On-line přístup:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC40125/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8570627/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.93.2.744
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Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP.

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