De novo mutation in the dopamine transporter gene associates dopamine dysfunction with autism spectrum disorder-Reference-Cited by-同舟云学术

De novo mutation in the dopamine transporter gene associates dopamine dysfunction with autism spectrum disorder

Published:2013-08-27 Issue:12 Volume:18 Page:1315-1323
ISSN:1359-4184
Container-title:Molecular Psychiatry
language:en
Short-container-title:Mol Psychiatry

Author:

Hamilton P J, ,Campbell N G,Sharma S,Erreger K,Herborg Hansen F,Saunders C,Belovich A N,Sahai M A,Cook E H,Gether U,Mchaourab H S,Matthies H J G,Sutcliffe J S,Galli A

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Molecular Biology

Link

http://www.nature.com/articles/mp2013102.pdf

Reference80 articles.

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3. Sanders SJ, Ercan-Sencicek AG, Hus V, Luo R, Murtha MT, Moreno-De-Luca D et al. Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. Neuron 2011; 70: 863–885.

4. Sebat J, Lakshmi B, Malhotra D, Troge J, Lese-Martin C, Walsh T et al. Strong association of de novo copy number mutations with autism. Science 2007; 316: 445–449.

5. Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R et al. Functional impact of global rare copy number variation in autism spectrum disorders. Nature 2010; 466: 368–372.

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