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GRIN3B missense mutation as an inherited risk factor for schizophrenia: whole-exome sequencing in a family with a familiar history of psychotic disorders
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GRIN3B missense mutation as an inherited risk factor for schizophrenia: whole-exome sequencing in a family with a familiar history of psychotic disorders

Genetical research, 2017-01, Vol.99, p.e1-e1, Article e1

Copyright © Cambridge University Press 2017 ;Copyright © Cambridge University Press 2017 This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited. ;Cambridge University Press 2017 2017 Cambridge University Press ;ISSN: 0016-6723 ;EISSN: 1469-5073 ;DOI: 10.1017/S0016672316000148 ;PMID: 28132660

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