Supportive Evidence for Reduced Expression of GNB1L in Schizophrenia-Reference-Cited by-同舟云学术

Supportive Evidence for Reduced Expression of GNB1L in Schizophrenia

Published:2008-11-14 Issue:4 Volume:36 Page:756-765
ISSN:1745-1701
Container-title:Schizophrenia Bulletin
language:en
Short-container-title:

Author:

Ishiguro Hiroki,Koga Minori,Horiuchi Yasue,Noguchi Emiko,Morikawa Miyuki,Suzuki Yoshimi,Arai Makoto,Niizato Kazuhiro,Iritani Shyuji,Itokawa Masanari,Inada Toshiya,Iwata Nakao,Ozaki Norio,Ujike Hiroshi,Kunugi Hiroshi,Sasaki Tsukasa,Takahashi Makoto,Watanabe Yuichiro,Someya Toshiyuki,Kakita Akiyoshi,Takahashi Hitoshi,Nawa Hiroyuki,Arinami Tadao

Publisher

Oxford University Press (OUP)

Subject

Psychiatry and Mental health

Link

http://academic.oup.com/schizophreniabulletin/article-pdf/36/4/756/16703909/sbn160.pdf

Reference36 articles.

1. 22q11 deletion syndrome: a genetic subtype of schizophrenia;Bassett;Biol Psychiatry,1999

2. The molecular genetics of the 22q11-associated schizophrenia;Karayiorgou;Brain Res Mol Brain Res,2004

3. Der(22) syndrome and velo-cardio-facial syndrome/DiGeorge syndrome share a 1.5-Mb region of overlap on chromosome 22q11;Funke;Am J Hum Genet,1999

4. Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis;Shaikh;Hum Mol Genet,2000

5. Role of TBX1 in human del22q11.2 syndrome;Yagi;Lancet,2003

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