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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...

詳細記述

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書誌詳細
出版年:Neuroscience
主要な著者: Wen, Teresa H., Lovelace, Jonathan W., Ethell, Iryna M., Binder, Devin K., Razak, Khaleel A.
フォーマット: Artigo
言語:Inglês
出版事項: 2018
主題:
オンライン・アクセス: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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