Retiring the term FTDP-17 as MAPT mutations are genetic forms of sporadic frontotemporal tauopathies

See Josephs (doi:10.1093/brain/awx367) for a scientific commentary on this article. In many neurodegenerative disorders, familial forms have provided important insights into the pathogenesis of their corresponding sporadic forms. The first mutations associated with frontotemporal lobar degeneration...

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Detalles Bibliográficos
Autores principales: Forrest, Shelley L, Kril, Jillian J, Stevens, Claire H, Kwok, John B, Hallupp, Marianne, Kim, Woojin S, Huang, Yue, McGinley, Ciara V, Werka, Hellen, Kiernan, Matthew C, Götz, Jürgen, Spillantini, Maria Grazia, Hodges, John R, Ittner, Lars M, Halliday, Glenda M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5888940/
https://www.ncbi.nlm.nih.gov/pubmed/29253099
http://dx.doi.org/10.1093/brain/awx328

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5888940/
https://www.ncbi.nlm.nih.gov/pubmed/29253099
http://dx.doi.org/10.1093/brain/awx328

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