Association between autism and variants in the wingless-type MMTV integration site family member 2 ( WNT2) gene-Reference-Cited by-同舟云学术

Association between autism and variants in the wingless-type MMTV integration site family member 2 ( WNT2) gene

Published:2009-11-09 Issue:04 Volume:13 Page:443
ISSN:1461-1457
Container-title:The International Journal of Neuropsychopharmacology
language:en
Short-container-title:Int. J. Neuropsychopharm.

Author:

Marui Tetsuya,Funatogawa Ikuko,Koishi Shinko,Yamamoto Kenji,Matsumoto Hideo,Hashimoto Ohiko,Jinde Seiichiro,Nishida Hisami,Sugiyama Toshiro,Kasai Kiyoto,Watanabe Keiichiro,Kano Yukiko,Kato Nobumasa

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Psychiatry and Mental health,Pharmacology

Link

http://academic.oup.com/ijnp/article-pdf/13/4/443/2101640/13-4-443.pdf

Reference23 articles.

1. The NOTCH4 locus is associated with susceptibility to schizophrenia

2. MECHANISMS OF WNT SIGNALING IN DEVELOPMENT

3. Identification of a Novel Gene on Chromosome 7q31 That Is Interrupted by a Translocation Breakpoint in an Autistic Individual

4. Xwnt-2b is a novel axis-inducing Xenopus Wnt, which is expressed in embryonic brain

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