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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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| Pubblicato in: | Curr Opin Genet Dev |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Elsevier
2021
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| Soggetti: | |
| Accesso online: | 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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