Modulation of mu attenuation to social stimuli in children and adults with 16p11.2 deletions and duplications

BACKGROUND: Copy number variations (CNV) within the recurrent ~600 kb chromosomal locus of 16p11.2 are associated with a wide range of neurodevelopmental disorders, including autism spectrum disorder (ASD). However, little is known about the social brain phenotype of 16p11.2 CNV and how this phenoty...

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Detalles Bibliográficos
Autores principales: Hudac, Caitlin M., Kresse, Anna, Aaronson, Benjamin, DesChamps, Trent D., Webb, Sara Jane, Bernier, Raphael A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4514956/
https://www.ncbi.nlm.nih.gov/pubmed/26213586
http://dx.doi.org/10.1186/s11689-015-9118-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4514956/
https://www.ncbi.nlm.nih.gov/pubmed/26213586
http://dx.doi.org/10.1186/s11689-015-9118-5

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