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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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| Publié dans: | Neuroscience |
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| Auteurs principaux: | , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
2018
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| Sujets: | |
| Accès en ligne: | 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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