De novo Mutations in Schizophrenia Implicate Chromatin Remodeling and Support a Genetic Overlap with Autism and Intellectual Disability

Schizophrenia is a serious psychiatric disorder with a broadly undiscovered genetic etiology. Recent studies of de novo mutations (DNM) in schizophrenia and autism have reinforced the hypothesis that rare genetic variation contributes to risk. We carried out exome sequencing on 57 trios with sporadi...

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主要な著者: McCarthy, Shane E., Gillis, Jesse, Kramer, Melissa, Lihm, Jayon, Yoon, Seungtai, Berstein, Yael, Mistry, Meeta, Pavlidis, Paul, Solomon, Rebecca, Ghiban, Elena, Antoniou, Eric, Kelleher, Eric, O’Brien, Carol, Donohoe, Gary, Gill, Michael, Morris, Derek W., McCombie, W. Richard., Corvin, Aiden
フォーマット: Artigo
言語:Inglês
出版事項: 2014
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Article
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4031262/
https://ncbi.nlm.nih.gov/pubmed/24776741
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/mp.2014.29
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