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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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| Yayımlandı: | Curr Opin Genet Dev |
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| Asıl Yazarlar: | , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Elsevier
2021
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| Konular: | |
| Online Erişim: | 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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