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Antisense Oligonucleotide Mediated Splice Correction of a Deep Intronic Mutation in OPA1
Inherited optic neuropathies (ION) present an important cause of blindness in the European working-age population. Recently we reported the discovery of four independent families with deep intronic mutations in the main inherited optic neuropathies gene OPA1. These deep intronic mutations cause mis-...
में बचाया:
| में प्रकाशित: | Mol Ther Nucleic Acids |
|---|---|
| मुख्य लेखकों: | , , , , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Nature Publishing Group
2016
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5155325/ https://ncbi.nlm.nih.gov/pubmed/27874857 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/mtna.2016.93 |
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