Abnormal auditory and language pathways in children with 16p11.2 deletion

Copy number variations at chromosome 16p11.2 contribute to neurodevelopmental disorders, including autism spectrum disorder (ASD). This study seeks to improve our understanding of the biological basis of behavioral phenotypes common in ASD, in particular the prominent and prevalent disruption of spo...

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Bibliographic Details
Published in:Neuroimage Clin
Main Authors: Berman, Jeffrey I., Chudnovskaya, Darina, Blaskey, Lisa, Kuschner, Emily, Mukherjee, Pratik, Buckner, Randall, Nagarajan, Srikantan, Chung, Wendy K., Spiro, John E., Sherr, Elliott H., Roberts, Timothy P.L.
Format: Artigo
Language:Inglês
Published: Elsevier 2015
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Regular Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4543079/
https://ncbi.nlm.nih.gov/pubmed/26413471
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nicl.2015.07.006
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