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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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| Publicado no: | J Neurodev Disord |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2019
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| Assuntos: | |
| 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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