Rare loss of function mutations in N-methyl-D-aspartate glutamate receptors and their contributions to schizophrenia susceptibility. (Q47873505)

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8 April 2020

title

Rare loss of function mutations in N-methyl-D-aspartate glutamate receptors and their contributions to schizophrenia susceptibility (English)

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8 April 2020

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29

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Daisuke Mori

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Yuko Arioka

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Tomoko Shiino

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Takashi Okada

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Masashi Ikeda

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Nakao Iwata

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T Oya-Ito

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Branko Aleksic

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Akira Yoshimi

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8

Miho Toyama

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Hiroki Kimura

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Mako Morikawa

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Yuko Okahisa

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4

Chenyao Wang

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14

Yukako Nakamura

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3

Yuto Takasaki

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6

Jingrui Xing

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Kanako Ishizuka

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Yota Uno

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20

Manabu Takaki

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24

Masahide Usami

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25

Masaki Kodaira

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author name string

Yanjie Yu

1

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Yingni Lin

2

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Shinji Sakamoto

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Toshiyuki Someya

22

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Jun Egawa

23

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language of work or name

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10 January 2018

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8 April 2020

published in

Translational Psychiatry

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volume

8

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page(s)

12

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issue

1

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Creative Commons Attribution 4.0 International

8 April 2020

copyright license

start time

10 January 2018

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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exact match

https://scigraph.springernature.com/pub.10.1038/s41398-017-0061-y

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22 May 2018

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22 May 2018

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22 May 2018

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22 May 2018

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22 May 2018

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22 May 2018

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22 May 2018

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22 May 2018

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22 May 2018

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14 August 2018

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14 August 2018

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14 August 2018

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14 August 2018

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21 January 2018

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7 January 2021

Duplications at 19q13.33 in patients with neurodevelopmental disorders.

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A recently-discovered NMDA receptor gene, GRIN3B, is associated with duration mismatch negativity

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7 January 2021

10.1038/S41398-017-0061-Y

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8 April 2020

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