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CNVs leading to fusion transcripts in individuals with autism spectrum disorder
There is strong evidence that rare copy number variants (CNVs) have a role in susceptibility to autism spectrum disorders (ASDs). Much research has focused on how CNVs mediate a phenotypic effect by altering gene expression levels. We investigated an alternative mechanism whereby CNVs combine the 5′...
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| 主要な著者: | , , , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Nature Publishing Group
2012
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3476715/ https://ncbi.nlm.nih.gov/pubmed/22549408 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2012.73 |
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