Shifted phase of EEG cross-frequency coupling in individuals with Phelan-McDermid syndrome

BACKGROUND: Phelan-McDermid Syndrome (PMS) is a rare condition caused by deletion or mutation of the SHANK3 gene. Individuals with PMS frequently present with intellectual disability, autism spectrum disorder, and other neurodevelopmental challenges. Electroencephalography (EEG) can provide a window...

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Detalles Bibliográficos
Autores principales: Mariscal, Michael. G., Berry-Kravis, Elizabeth, Buxbaum, Joseph D., Ethridge, Lauren E., Filip-Dhima, Rajna, Foss-Feig, Jennifer H., Kolevzon, Alexander, Modi, Meera. E., Mosconi, Matthew W., Nelson, Charles A., Powell, Craig M., Siper, Paige M., Soorya, Latha, Thaliath, Andrew, Thurm, Audrey, Zhang, Bo, Sahin, Mustafa, Levin, April R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8082621/
https://www.ncbi.nlm.nih.gov/pubmed/33910615
http://dx.doi.org/10.1186/s13229-020-00411-9

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