Microglia in frontotemporal lobar degeneration with progranulin or C9ORF72 mutations

OBJECTIVE: To identify clinicopathological differences between frontotemporal lobar degeneration (FTLD) due to mutations in progranulin (FTLD‐GRN) and chromosome 9 open reading frame 72 (FTLD‐C9ORF72). METHODS: We performed quantitative neuropathologic comparison of 17 FTLD‐C9ORF72 and 15 FTLD‐GRN w...

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Detalles Bibliográficos
Autores principales: Sakae, Nobutaka, Roemer, Shanu F., Bieniek, Kevin F., Murray, Melissa E., Baker, Matthew C., Kasanuki, Koji, Graff‐Radford, Neill R., Petrucelli, Leonard, Van Blitterswijk, Marka, Rademakers, Rosa, Dickson, Dennis W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764493/
https://www.ncbi.nlm.nih.gov/pubmed/31448566
http://dx.doi.org/10.1002/acn3.50875

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764493/
https://www.ncbi.nlm.nih.gov/pubmed/31448566
http://dx.doi.org/10.1002/acn3.50875

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