CHD8 haploinsufficiency results in autistic-like phenotypes in mice-Reference-Cited by-同舟云学术

CHD8 haploinsufficiency results in autistic-like phenotypes in mice

Published:2016-09 Issue:7622 Volume:537 Page:675-679
ISSN:0028-0836
Container-title:Nature
language:en
Short-container-title:Nature

Author:

Katayama Yuta,Nishiyama Masaaki,Shoji Hirotaka,Ohkawa Yasuyuki,Kawamura Atsuki,Sato Tetsuya,Suyama Mikita,Takumi Toru,Miyakawa Tsuyoshi,Nakayama Keiichi I.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/nature19357.pdf

Reference46 articles.

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

3. Iossifov, I. et al. De novo gene disruptions in children on the autistic spectrum. Neuron 74, 285–299 (2012)

4. O’Roak, B. J. et al. Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations. Nature 485, 246–250 (2012)

5. Talkowski, M. E. et al. Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries. Cell 149, 525–537 (2012)

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