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

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
Main Authors: Jeffrey I. Berman, Darina Chudnovskaya, Lisa Blaskey, Emily Kuschner, Pratik Mukherjee, Randall Buckner, Srikantan Nagarajan, Wendy K. Chung, John E. Spiro, Elliott H. Sherr, Timothy P.L. Roberts
Format: Article
Language:English
Published: Elsevier 2015-01-01
Series:NeuroImage: Clinical
Subjects:
16p11.2 deletion
Diffusion MR
Auditory system
Arcuate fasciculus
Language
Autism
Online Access:http://www.sciencedirect.com/science/article/pii/S2213158215001254

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http://www.sciencedirect.com/science/article/pii/S2213158215001254

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