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Antisense oligonucleotides: A primer
There are few disease-modifying therapeutics for neurodegenerative diseases, but successes on the development of antisense oligonucleotide (ASO) therapeutics for spinal muscular atrophy and Duchenne muscular dystrophy predict a robust future for ASOs in medicine. Indeed, existing pipelines for the d...
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| Udgivet i: | Neurol Genet |
|---|---|
| Main Authors: | , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Wolters Kluwer
2019
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6501637/ https://ncbi.nlm.nih.gov/pubmed/31119194 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/NXG.0000000000000323 |
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