Opposing Brain Differences in 16p11.2 Deletion and Duplication Carriers

Deletions and duplications of the recurrent ∼600 kb chromosomal BP4–BP5 region of 16p11.2 are associated with a broad variety of neurodevelopmental outcomes including autism spectrum disorder. A clue to the pathogenesis of the copy number variant (CNV)'s effect on the brain is that the deletion...

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Main Authors: Qureshi, Abid Y., Mueller, Sophia, Snyder, Abraham Z., Mukherjee, Pratik, Berman, Jeffrey I., Roberts, Timothy P.L., Nagarajan, Srikantan S., Spiro, John E., Chung, Wendy K., Sherr, Elliott H., Buckner, Randy L.
Formato: Artigo
Idioma:Inglês
Publicado em: Society for Neuroscience 2014
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4138332/
https://ncbi.nlm.nih.gov/pubmed/25143601
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.1366-14.2014
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