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Article

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

Neurobiology of disease - 1 Jul 2018

Lovelace Jonathan W, Ethell Iryna M, Binder Devin K, Razak Khaleel A

Abstract excerpt

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 increased anxiety, social and sensory processing deficits. Recent EEG studies in humans with FXS have identified neural...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 29605426
DOI: 10.1016/j.nbd.2018.03.012
PMCID: PMC5969806

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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