Social cognition in 22q11.2 deletion syndrome and idiopathic developmental neuropsychiatric disorders

BACKGROUND: 22q11.2 deletion syndrome (22q11DS) is a common recurrent neurogenetic condition associated with elevated risk for developmental neuropsychiatric disorders and intellectual disability. Children and adults with 22q11DS often exhibit marked social impairment as well as neurocognitive defic...

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Detalles Bibliográficos
Autores principales: Jalal, Rhideeta, Nair, Aarti, Lin, Amy, Eckfeld, Ariel, Kushan, Leila, Zinberg, Jamie, Karlsgodt, Katherine H., Cannon, Tyrone D., Bearden, Carrie E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8052741/
https://www.ncbi.nlm.nih.gov/pubmed/33863277
http://dx.doi.org/10.1186/s11689-021-09363-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8052741/
https://www.ncbi.nlm.nih.gov/pubmed/33863277
http://dx.doi.org/10.1186/s11689-021-09363-4

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