Neurofibrillary tangles in Gerstmann-Sträussler-Scheinker syndrome with the A117V prion gene mutation

One patient of a French family with Gerstmann-Sträussler-Scheinker syndrome with the mutation in codon 117 of the prion protein (PrP) gene displayed unexpected neuritic degeneration around PrP plaques and numerous diffuse neurofibrillary tangles, whereas other members did not. The tau profile in thi...

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Hlavní autoři: Tranchant, C, Sergeant, N, Wattez, A, Mohr, M, Warter, J, Delacourte, A
Médium: Artigo
Jazyk:Inglês
Vydáno: BMJ Group 1997
Témata:
Short Report
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2169673/
https://ncbi.nlm.nih.gov/pubmed/9285466
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