Delta power robustly predicts cognitive function in Angelman syndrome

OBJECTIVE: Angelman syndrome (AS) is a severe neurodevelopmental disorder caused by loss of function of the maternally inherited UBE3A gene in neurons. Promising disease‐modifying treatments to reinstate UBE3A expression are under development and an early measure of treatment response is critical to...

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Detalles Bibliográficos
Autores principales: Ostrowski, Lauren M., Spencer, Elizabeth R., Bird, Lynne M., Thibert, Ronald, Komorowski, Robert W., Kramer, Mark A., Chu, Catherine J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8283185/
https://www.ncbi.nlm.nih.gov/pubmed/34047077
http://dx.doi.org/10.1002/acn3.51385

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8283185/
https://www.ncbi.nlm.nih.gov/pubmed/34047077
http://dx.doi.org/10.1002/acn3.51385

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