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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Detalles Bibliográficos
Autores principales: Roche, Katherine J., LeBlanc, Jocelyn J., Levin, April R., O’Leary, Heather M., Baczewski, Lauren M., Nelson, Charles A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6668116/
https://www.ncbi.nlm.nih.gov/pubmed/31362710
http://dx.doi.org/10.1186/s11689-019-9275-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6668116/
https://www.ncbi.nlm.nih.gov/pubmed/31362710
http://dx.doi.org/10.1186/s11689-019-9275-z

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