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...

ver descrição completa

Detalhes bibliográficos

Principais autores:	N. A. Copping, J. L. Silverman
Formato:	Artigo
Idioma:	Inglês
Publicado em:	BMC 2021-02-01
coleção:	Molecular Autism
Assuntos:	Genetics Mouse models Seizures Sleep Behavior Angelman Syndrome
Acesso em linha:	https://doi.org/10.1186/s13229-021-00416-y
Tags:	Adicionar Tag Sem tags, seja o primeiro a adicionar uma tag!