Impact of the genome wide supported NRGN gene on anterior cingulate morphology in schizophrenia.

BACKGROUND: The rs12807809 single-nucleotide polymorphism in NRGN is a genetic risk variant with genome-wide significance for schizophrenia. The frequency of the T allele of rs12807809 is higher in individuals with schizophrenia than in those without the disorder. Reduced immunoreactivity of NRGN, w...

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Bibliographic Details
Main Authors: Kazutaka Ohi, Ryota Hashimoto, Yuka Yasuda, Kiyotaka Nemoto, Takashi Ohnishi, Motoyuki Fukumoto, Hidenaga Yamamori, Satomi Umeda-Yano, Takeya Okada, Masao Iwase, Hiroaki Kazui, Masatoshi Takeda
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3257237?pdf=render