Refining the Behavioral Phenotype of Angelman Syndrome: Examining Differences in Motivation for Social Contact Between Genetic Subgroups

Angelman syndrome (AS) is caused by loss of information from the 15q11.2-13 region on the maternal chromosome with striking phenotypic difference from Prader–Willi syndrome in which information is lost from the same region on the paternal chromosome. Motivation for social contact and sensory seeking...

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Detalles Bibliográficos
Autores principales: Heald, Mary, Adams, Dawn, Walls, Emily, Oliver, Christopher
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7921159/
https://www.ncbi.nlm.nih.gov/pubmed/33664655
http://dx.doi.org/10.3389/fnbeh.2021.618271

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7921159/
https://www.ncbi.nlm.nih.gov/pubmed/33664655
http://dx.doi.org/10.3389/fnbeh.2021.618271

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