Network degeneration and dysfunction in presymptomatic C9ORF72 expansion carriers

Hexanucleotide repeat expansions in C9ORF72 are the most common known genetic cause of familial and sporadic frontotemporal dementia and amyotrophic lateral sclerosis. Previous work has shown that patients with behavioral variant frontotemporal dementia due to C9ORF72 show salience and sensorimotor...

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Detalles Bibliográficos
Autores principales: Lee, Suzee E., Sias, Ana C., Mandelli, Maria Luisa, Brown, Jesse A., Brown, Alainna B., Khazenzon, Anna M., Vidovszky, Anna A., Zanto, Theodore P., Karydas, Anna M., Pribadi, Mochtar, Dokuru, Deepika, Coppola, Giovanni, Geschwind, Dan H., Rademakers, Rosa, Gorno-Tempini, Maria Luisa, Rosen, Howard J., Miller, Bruce L., Seeley, William W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Regular Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5349617/
https://www.ncbi.nlm.nih.gov/pubmed/28337409
http://dx.doi.org/10.1016/j.nicl.2016.12.006

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5349617/
https://www.ncbi.nlm.nih.gov/pubmed/28337409
http://dx.doi.org/10.1016/j.nicl.2016.12.006

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