Abnormal electrophysiological phenotypes and sleep deficits in a mouse model of Angelman Syndrome
Abstract Background Angelman Syndrome (AS) is a rare genetic disorder characterized by impaired communication, motor and balance deficits, intellectual disabilities, recurring seizures and abnormal sleep patterns. The genetic cause of AS is neuronal-specific loss of expression of UBE3A (ubiquitin-pr...
Main Authors: | , |
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Format: | Article |
Language: | English |
Published: |
BMC
2021-02-01
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Series: | Molecular Autism |
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Online Access: | https://doi.org/10.1186/s13229-021-00416-y |