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: | N. A. Copping, J. L. Silverman |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2021-02-01
|
Series: | Molecular Autism |
Subjects: | |
Online Access: | https://doi.org/10.1186/s13229-021-00416-y |
Similar Items
-
Vigabatrin-Induced Seizures in Angelman Syndrome
by: J Gordon Millichap
Published: (1998-12-01) -
Delayed loss of UBE3A reduces the expression of Angelman syndrome-associated phenotypes
by: Monica Sonzogni, et al.
Published: (2019-05-01) -
Epilepsy in Angelman’s Syndrome
by: J Gordon Millichap
Published: (2009-12-01) -
Angelman Syndrome: Chromosome Abnormality
by: J Gordon Millichap
Published: (1992-12-01) -
Electrophysiological Abnormalities in Angelman Syndrome Correlate With Symptom Severity
by: Joerg F. Hipp, et al.
Published: (2021-09-01)