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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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Detalles Bibliográficos
Autores principales:	Ohi, Kazutaka, Hashimoto, Ryota, Yasuda, Yuka, Nemoto, Kiyotaka, Ohnishi, Takashi, Fukumoto, Motoyuki, Yamamori, Hidenaga, Umeda-Yano, Satomi, Okada, Takeya, Iwase, Masao, Kazui, Hiroaki, Takeda, Masatoshi
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2012
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3257237/ https://www.ncbi.nlm.nih.gov/pubmed/22253779 http://dx.doi.org/10.1371/journal.pone.0029780

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