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Epilepsy in Angelman syndrome: A Scoping Review
Angelman Syndrome (AS) is characterized by severe developmental delays including marked speech impairment, movement abnormalities(ataxia, tremor), and unique behaviors such as frequent laughter and is caused by dysfunctional maternal UBE3A gene (maternal 15q11–13 deletions, maternal specific UBE3A m...
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| Published in: | Brain Dev |
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| Main Author: | |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
2020
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| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7688500/ https://ncbi.nlm.nih.gov/pubmed/32893075 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.braindev.2020.08.014 |
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