Rare loss of function mutations in N-methyl-d-aspartate glutamate receptors and their contributions to schizophrenia susceptibility-Reference-Cited by-同舟云学术

Rare loss of function mutations in N-methyl-d-aspartate glutamate receptors and their contributions to schizophrenia susceptibility

Published:2018-01-10 Issue:1 Volume:8 Page:
ISSN:2158-3188
Container-title:Translational Psychiatry
language:en
Short-container-title:Transl Psychiatry

Author:

Yu Yanjie,Lin Yingni,Takasaki Yuto,Wang Chenyao,Kimura Hiroki,Xing Jingrui,Ishizuka Kanako,Toyama Miho,Kushima Itaru,Mori Daisuke,Arioka Yuko,Uno Yota,Shiino Tomoko,Nakamura Yukako,Okada Takashi,Morikawa Mako,Ikeda Masashi,Iwata Nakao,Okahisa Yuko,Takaki Manabu,Sakamoto Shinji,Someya Toshiyuki,Egawa Jun,Usami Masahide,Kodaira Masaki,Yoshimi Akira,Oya-Ito Tomoko^ORCID,Aleksic Branko^ORCID,Ohno Kinji,Ozaki Norio^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Biological Psychiatry,Cellular and Molecular Neuroscience,Psychiatry and Mental health

Link

http://www.nature.com/articles/s41398-017-0061-y.pdf

Reference54 articles.

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4. Sullivan, P. F., Kendler, K. S. & Neale, M. C. Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies. Arch. Gen. Psychiatry 60, 1187–1192 (2003).

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