Novel missense SETD1A variants in Japanese patients with schizophrenia: Resequencing and association analysis

Ryo Morikawa,Yuichiro Watanabe,Hirofumi Igeta,Reza K. Arta,Masashi Ikeda,Satoshi Okazaki,Satoshi Hoya,Takeo Saito,Ikuo Otsuka,Jun Egawa,Takaki Tanifuji,Nakao Iwata,Toshiyuki Someya

Psychiatry Research（2022）

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摘要

•We identified novel missense SETD1A variants exclusively in schizophrenia patients.•A schizophrenia patient with a p.Glu857Gln variant had developmental delays.•Novel missense SETD1A variants were not significantly associated with schizophrenia.

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关键词

Developmental delay,Genotyping,Rare variant,Schizophrenia,SETD1A

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