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Developmental changes in EEG phenotypes in a mouse model of Fragile X Syndrome

Fragile X Syndrome (FXS) is a leading genetic cause of autism and intellectual disabilities. Sensory processing deficits are common in humans with FXS and an animal model, the Fmr1 knockout (KO) mouse, manifesting in the auditory system as debilitating hypersensitivity and abnormal electroencephalog...

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Detalhes bibliográficos
Publicado no:Neuroscience
Main Authors: Wen, Teresa H., Lovelace, Jonathan W., Ethell, Iryna M., Binder, Devin K., Razak, Khaleel A.
Formato: Artigo
Idioma:Inglês
Publicado em: 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6331246/
https://ncbi.nlm.nih.gov/pubmed/30528856
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuroscience.2018.11.047
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