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An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArray
Autism spectrum disorder (ASD) is a neurodevelopmental condition with a complex and heterogeneous genetic etiology. While a proportion of ASD risk is attributable to common variants, rare copy-number variants (CNVs) and protein-disrupting single-nucleotide variants (SNVs) have been shown to signific...
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| 發表在: | Sci Rep |
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| Main Authors: | , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Nature Publishing Group UK
2020
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7035424/ https://ncbi.nlm.nih.gov/pubmed/32081867 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-020-59922-3 |
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