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Copy number variation and neuropsychiatric illness
Copy number variants (CNVs) at specific loci have been identified as important risk factors for several neuropsychiatric disorders, such as schizophrenia, autism spectrum disorder, intellectual disability (ID) and depression. These CNVs are individually rare (<0.5% frequency), have high effect si...
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| 發表在: | Curr Opin Genet Dev |
|---|---|
| Main Authors: | , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Elsevier
2021
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8219524/ https://ncbi.nlm.nih.gov/pubmed/33752146 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.gde.2021.02.014 |
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