A resting EEG study of neocortical hyperexcitability and altered functional connectivity in fragile X syndrome

BACKGROUND: Cortical hyperexcitability due to abnormal fast-spiking inhibitory interneuron function has been documented in fmr1 KO mice, a mouse model of the fragile X syndrome which is the most common single gene cause of autism and intellectual disability. METHODS: We collected resting state dense...

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Detalhes bibliográficos
Publicado no:J Neurodev Disord
Main Authors: Wang, Jun, Ethridge, Lauren E., Mosconi, Matthew W., White, Stormi P., Binder, Devin K., Pedapati, Ernest V., Erickson, Craig A., Byerly, Matthew J., Sweeney, John A.
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2017
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5351111/
https://ncbi.nlm.nih.gov/pubmed/28316753
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s11689-017-9191-z
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