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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Elsevier
2020
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| Materias: | |
| 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 |