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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Detalhes bibliográficos
Publicado no: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.
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2015
Assuntos:
Regular Article
Acesso em linha: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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