載入...
Future directions for high-throughput splicing assays in precision medicine
Classification of variants of unknown significance is a challenging technical problem in clinical genetics. As up to one third of disease-causing mutations are thought to affect pre-mRNA splicing, it is important to accurately classify splicing mutations in patient sequencing data. Several consortia...
Na minha lista:
| 發表在: | Hum Mutat |
|---|---|
| Main Authors: | , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
2019
|
| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6744296/ https://ncbi.nlm.nih.gov/pubmed/31297895 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.23866 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|