Communication‐related assessments in an Angelman syndrome mouse model

INTRODUCTION: Angelman syndrome (AS) is a neurodevelopmental disorder characterized by motor deficits, seizures, some autistic‐like behaviors, and severe impairment of speech. A dysfunction of the maternally imprinted UBE3A gene, coupled with a functional yet silenced paternal copy, results in AS. A...

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Detalles Bibliográficos
Autores principales: Perrino, Peter A., Chamberlain, Stormy J., Eigsti, Inge‐Marie, Fitch, Roslyn Holly
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7821623/
https://www.ncbi.nlm.nih.gov/pubmed/33151040
http://dx.doi.org/10.1002/brb3.1937

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7821623/
https://www.ncbi.nlm.nih.gov/pubmed/33151040
http://dx.doi.org/10.1002/brb3.1937

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