Altered network connectivity in frontotemporal dementia with C9orf72 hexanucleotide repeat expansion

Hexanucleotide repeat expansion in C9orf72 represents the most common genetic cause of familial and sporadic behavioural variant frontotemporal dementia. Previous studies show that some C9orf72 carriers with behavioural variant frontotemporal dementia exhibit distinctive atrophy patterns whereas oth...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Lee, Suzee E., Khazenzon, Anna M., Trujillo, Andrew J., Guo, Christine C., Yokoyama, Jennifer S., Sha, Sharon J., Takada, Leonel T., Karydas, Anna M., Block, Nikolas R., Coppola, Giovanni, Pribadi, Mochtar, Geschwind, Daniel H., Rademakers, Rosa, Fong, Jamie C., Weiner, Michael W., Boxer, Adam L., Kramer, Joel H., Rosen, Howard J., Miller, Bruce L., Seeley, William W.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2014
Assuntos:
Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4208465/
https://ncbi.nlm.nih.gov/pubmed/25273996
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awu248
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados