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

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

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Veröffentlicht in:Journal of neurodevelopmental disorders 2017-03, Vol.9 (1), p.11, Article 11
Hauptverfasser: 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
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Sprache:eng
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