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Translation-relevant EEG phenotypes in a mouse model of Fragile X Syndrome

Identification of comparable biomarkers in humans and validated animal models will facilitate pre-clinical to clinical therapeutic pipelines to treat neurodevelopmental disorders. Fragile X Syndrome (FXS) is a leading known genetic cause of intellectual disability with symptoms that include increase...

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Detaylı Bibliyografya
Yayımlandı:Neurobiol Dis
Asıl Yazarlar: Lovelace, Jonathan W., Ethell, Iryna M., Binder, Devin K., Razak, Khaleel A.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2018
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5969806/
https://ncbi.nlm.nih.gov/pubmed/29605426
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2018.03.012
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