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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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: 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.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Society for Neuroscience 2014
Pynciau:
Articles
Mynediad Ar-lein: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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