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Pathogenic variants that alter protein code often disrupt splicing
The lack of tools to identify causative variants from sequencing data greatly limits the promise of Precision Medicine. Previous studies suggest one-third of disease alleles alter splicing. We discovered that splicing defects cluster in diseases (e.g. haploinsufficient genes). We analyzed 4,964 publ...
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| 出版年: | Nat Genet |
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| 主要な著者: | , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2017
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6679692/ https://ncbi.nlm.nih.gov/pubmed/28416821 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.3837 |
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