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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Detalhes bibliográficos
Publicado no:Ann Clin Transl Neurol
Main Authors: Ostrowski, Lauren M., Spencer, Elizabeth R., Bird, Lynne M., Thibert, Ronald, Komorowski, Robert W., Kramer, Mark A., Chu, Catherine J.
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2021
Assuntos:
Research Articles
Acesso em linha: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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