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Sequencing of selected chromatin remodelling genes reveals increased burden of rare missense variants in ASD patients from the Japanese population.

International review of psychiatry (Abingdon, England) - 17 Feb 2022

Lo Tzuyao, Kushima Itaru, Aleksic Branko, Kato Hidekazu, Nawa Yoshihiro, Hayashi Yu, Otgonbayar Gantsooj, Kimura Hiroki, Arioka Yuko, Mori Daisuke, Ozaki Norio

Abstract excerpt

Chromatin remodelling is an important process in neural development and is related to autism spectrum disorder (ASD) and schizophrenia (SCZ) aetiology. To further elucidate the involvement of chromatin remodelling genes in the genetic aetiology of ASD and SCZ in the Japanese population, we performed a case-control study. Targeted sequencing was conducted on coding regions of four BAF chromatin remodelling complex...

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PMID: 35699097
DOI: 10.1080/09540261.2022.2072193

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

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