Reviewing Evidence for the Relationship of EEG Abnormalities and RTT Phenotype Paralleled by Insights from Animal Studies

Rett syndrome (RTT) is a rare neurodevelopmental disorder that is usually caused by mutations of the MECP2 gene. Patients with RTT suffer from severe deficits in motor, perceptual and cognitive domains. Electroencephalogram (EEG) has provided useful information to clinicians and scientists, from the...

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Detalles Bibliográficos
Autores principales: Smirnov, Kirill, Stroganova, Tatiana, Molholm, Sophie, Sysoeva, Olga
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8157853/
https://www.ncbi.nlm.nih.gov/pubmed/34069993
http://dx.doi.org/10.3390/ijms22105308

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8157853/
https://www.ncbi.nlm.nih.gov/pubmed/34069993
http://dx.doi.org/10.3390/ijms22105308

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