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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Enregistré dans:
Détails bibliographiques
Publié dans:Ann Clin Transl Neurol
Auteurs principaux: Ostrowski, Lauren M., Spencer, Elizabeth R., Bird, Lynne M., Thibert, Ronald, Komorowski, Robert W., Kramer, Mark A., Chu, Catherine J.
Format: Artigo
Langue:Inglês
Publié: John Wiley and Sons Inc. 2021
Sujets:
Research Articles
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC8283185/
https://ncbi.nlm.nih.gov/pubmed/34047077
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.51385
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