Loss of Wdfy3 in mice alters cerebral cortical neurogenesis reflecting aspects of the autism pathology-Reference-Cited by-同舟云学术

Loss of Wdfy3 in mice alters cerebral cortical neurogenesis reflecting aspects of the autism pathology

Published:2014-09-08 Issue:1 Volume:5 Page:
ISSN:2041-1723
Container-title:Nature Communications
language:en
Short-container-title:Nat Commun

Author:

Orosco Lori A.,Ross Adam P.,Cates Staci L.,Scott Sean E.,Wu Dennis,Sohn Jiho,Pleasure David,Pleasure Samuel J.,Adamopoulos Iannis E.,Zarbalis Konstantinos S

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

Link

http://www.nature.com/articles/ncomms5692.pdf

Reference70 articles.

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3. O'Roak, B. J. et al. Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. Nat. Genet. 43, 585–589 (2011).

4. Sanders, S. J. et al. De novo mutations revealed by whole-exome sequencing are strongly associated with autism. Nature 485, 237–241 (2012).

5. Neale, B. M. et al. Patterns and rates of exonic de novo mutations in autism spectrum disorders. Nature 485, 242–245 (2012).

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