Analysis of the BTBD9 and HTR2C variants in Chinese Han patients with Tourette syndrome-Reference-Cited by-同舟云学术

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Analysis of the BTBD9 and HTR2C variants in Chinese Han patients with Tourette syndrome

Published:2012-12 Issue:6 Volume:22 Page:300-303
ISSN:0955-8829
Container-title:Psychiatric Genetics
language:en
Short-container-title:

Author:

Guo Yi,Su Linyan,Zhang Jie,Lei Jing,Deng Xiong,Xu Hongbo,Yang Zuocheng,Kuang Shoujin,Tang Jinsong,Luo Ziqiang,Deng Hao

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Biological Psychiatry,Psychiatry and Mental health,Genetics (clinical),Genetics

Reference33 articles.

1. Sequence variants in SLITRK1 are associated with Tourettes syndrome.;Abelson;Science,2005

2. Pharmacologic mechanisms of serotonergic regulation of dopamine neurotransmission.;Alex;Pharmacol Ther,2007

3. Genome scan for linkage to Gilles de la Tourette syndrome.;Barr;Am J Med Genet,1999

4. Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome.;Belloso;Eur J Hum Genet,2007

5. Tourette disorder spectrum maps to chromosome 14q31.1 in an Italian kindred.;Breedveld;Neurogenetics,2010

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