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Somatic Copy Number Variants in Neuropsychiatric Disorders
Copy number variants (CNVs) have been implicated in neuropsychiatric disorders, with rare-inherited and de novo CNVs (dnCNVs) having large effects on disease liability. Recent studies started exploring a class of dnCNVs that occur post-zygotically, and are therefore present in some but not all cells...
Sparad:
| I publikationen: | Curr Opin Genet Dev |
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| Huvudupphovsmän: | , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2021
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8205940/ https://ncbi.nlm.nih.gov/pubmed/33444936 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.gde.2020.12.013 |
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