Short-latency somatosensory-evoked potentials demonstrate cortical dysfunction in patients with Angelman syndrome

BACKGROUND: Angelman syndrome (AS) is neurodevelopmental disorder, causal gene of which is maternally expressed UBE3A. A majority of patients results from the large deletion of relevant chromosome which includes GABA(A) receptor subunit genes (GABARs) as well as UBE3A (AS Del). We previously reporte...

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Detalles Bibliográficos
Autores principales: Egawa, Kiyoshi, Saitoh, Shinji, Asahina, Naoko, Shiraishi, Hideaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7721653/
https://www.ncbi.nlm.nih.gov/pubmed/33313428
http://dx.doi.org/10.1016/j.ensci.2020.100298

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7721653/
https://www.ncbi.nlm.nih.gov/pubmed/33313428
http://dx.doi.org/10.1016/j.ensci.2020.100298

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