Supportive Evidence for Reduced Expression of GNB1L in Schizophrenia

Background: Chromosome 22q11 deletion syndrome (22q11DS) increases the risk of development of schizophrenia more than 10 times compared with that of the general population, indicating that haploinsufficiency of a subset of the more than 20 genes contained in the 22q11DS region could increase the ris...

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Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2010
Matèries:
Regular Articles
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2894596/
https://ncbi.nlm.nih.gov/pubmed/19011233
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/schbul/sbn160
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