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Large mosaic copy number variations confer autism risk
Although germline de novo copy number variants are known causes of autism spectrum disorder (ASD), the contribution of mosaic (early-developmental) copy number variants (mCNVs) has not been explored. Here, we assessed the contribution of mCNVs to ASD by ascertaining mCNVs in genotype array intensity...
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| Publicado no: | Nat Neurosci |
|---|---|
| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7854495/ https://ncbi.nlm.nih.gov/pubmed/33432194 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41593-020-00766-5 |
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