Rare compound heterozygous missense SPATA7 variations and risk of schizophrenia; whole-exome sequencing in a consanguineous family with affected siblings, follow-up sequencing and a case-control study

Rare compound heterozygous missense SPATA7 variations and risk of schizophrenia; whole-exome sequencing in a consanguineous family with affected siblings, follow-up sequencing and a case-control study

Hirofumi Igeta,1 Yuichiro Watanabe,1 Ryo Morikawa,1 Masashi Ikeda,2 Ikuo Otsuka,3 Satoshi Hoya,1 Masataka Koizumi,1 Jun Egawa,1 Akitoyo Hishimoto,3 Nakao Iwata,2 Toshiyuki Someya11Department of Psychiatry, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan; 2Department...

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Bibliographic Details
Main Authors:	Igeta H, Watanabe Y, Morikawa R, Ikeda M, Otsuka I, Hoya S, Koizumi M, Egawa J, Hishimoto A, Iwata N, Someya T
Format:	Article
Language:	English
Published:	Dove Medical Press 2019-08-01
Series:	Neuropsychiatric Disease and Treatment
Subjects:	Japanese multiplex schizophrenia family next-generation sequencing recessive variations
Online Access:	https://www.dovepress.com/rare-compound-heterozygous-missense-spata7-variations-and-risk-of-schi-peer-reviewed-article-NDT

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