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Double hits in schizophrenia
The co-occurrence of a copy number variant (CNV) and a functional variant on the other allele may be a relevant genetic mechanism in schizophrenia. We hypothesized that the cumulative burden of such double hits—in particular those composed of a deletion and a coding single-nucleotide variation (SNV)...
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| 出版年: | Hum Mol Genet |
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| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2018
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6049008/ https://ncbi.nlm.nih.gov/pubmed/29767709 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddy175 |
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