Two distinct prions in fatal familial insomnia and its sporadic form

Fatal familial insomnia is a genetic prion disease, which is associated with the aspartic acid to asparagine substitution at codon 178 of the prion protein gene. Although the hallmark pathological feature is thalamic and olivary degeneration, there is a patient with an atypical fatal familial insomn...

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Detalles Bibliográficos
Autores principales: Takeuchi, Atsuko, Mohri, Shirou, Kai, Hideaki, Tamaoka, Akira, Kobayashi, Atsushi, Mizusawa, Hidehiro, Iwasaki, Yasushi, Yoshida, Mari, Shimizu, Hiroshi, Murayama, Shigeo, Kuroda, Shigetoshi, Morita, Masanori, Parchi, Piero, Kitamoto, Tetsuyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7425372/
https://www.ncbi.nlm.nih.gov/pubmed/32954274
http://dx.doi.org/10.1093/braincomms/fcz045

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