Abnormal electrophysiological phenotypes and sleep deficits in a mouse model of Angelman Syndrome

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-protein li...

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Detalles Bibliográficos
Autores principales: Copping, N. A., Silverman, J. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7866697/
https://www.ncbi.nlm.nih.gov/pubmed/33549123
http://dx.doi.org/10.1186/s13229-021-00416-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7866697/
https://www.ncbi.nlm.nih.gov/pubmed/33549123
http://dx.doi.org/10.1186/s13229-021-00416-y

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