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...

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Bibliografische gegevens
Hoofdauteurs: 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.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Oxford University Press 2014
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Original Articles
Online toegang: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
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