載入...
AON-Mediated Exon Skipping to Bypass Protein Truncation in Retinal Dystrophies Due to the Recurrent CEP290 c.4723A > T Mutation. Fact or Fiction?
Mutations in CEP290 encoding a centrosomal protein important to cilia formation cause a spectrum of diseases, from isolated retinal dystrophies to multivisceral and sometimes embryo–lethal ciliopathies. In recent years, endogenous and/or selective non-canonical exon skipping of mutant exons have bee...
Na minha lista:
| 發表在: | Genes (Basel) |
|---|---|
| Main Authors: | , , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
MDPI
2019
|
| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6562928/ https://ncbi.nlm.nih.gov/pubmed/31091803 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes10050368 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|