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

PURPOSE: Whole-exome sequencing (WES) of multiplex families is a promising strategy for identifying causative variations for common diseases. To identify rare recessive risk variations for schizophrenia, we performed a WES study in a consanguineous family with affected siblings. We then performed fo...

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Detalhes bibliográficos
Publicado no:Neuropsychiatr Dis Treat
Main Authors: Igeta, Hirofumi, Watanabe, Yuichiro, Morikawa, Ryo, Ikeda, Masashi, Otsuka, Ikuo, Hoya, Satoshi, Koizumi, Masataka, Egawa, Jun, Hishimoto, Akitoyo, Iwata, Nakao, Someya, Toshiyuki
Formato: Artigo
Idioma:Inglês
Publicado em: Dove 2019
Assuntos:
Original Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6707433/
https://ncbi.nlm.nih.gov/pubmed/31695380
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/NDT.S218773
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