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Schizophrenia copy number variants and associative learning
Large-scale genomic studies have made major progress in identifying genetic risk variants for schizophrenia. A key finding from these studies is that there is an increased burden of genomic copy number variants (CNVs) in schizophrenia cases compared with controls. The mechanism through which these C...
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| 出版年: | Mol Psychiatry |
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| 主要な著者: | , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Nature Publishing Group
2017
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5285462/ https://ncbi.nlm.nih.gov/pubmed/27956746 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/mp.2016.227 |
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