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Electroencephalographic spectral power as a marker of cortical function and disease severity in girls with Rett syndrome

BACKGROUND: Rett syndrome is a neurodevelopmental disorder caused by a mutation in the X-linked MECP2 gene. Individuals with Rett syndrome typically develop normally until around 18 months of age before undergoing a developmental regression, and the disorder can lead to cognitive, motor, sensory, an...

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Detalhes bibliográficos
Publicado no:J Neurodev Disord
Main Authors: Roche, Katherine J., LeBlanc, Jocelyn J., Levin, April R., O’Leary, Heather M., Baczewski, Lauren M., Nelson, Charles A.
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2019
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6668116/
https://ncbi.nlm.nih.gov/pubmed/31362710
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s11689-019-9275-z
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