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CRISPR challenges in treating retinal disease
Ophthalmic researchers and clinicians arguably have led the way for safe, effective gene therapy, most notably with adeno-associated viral gene supplementation in the treatment of Leber congenital amaurosis type 2 (LCA 2) patients with mutations in the RPE65 gene. These successes notwithstanding, mo...
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| I publikationen: | Asia Pac J Ophthalmol (Phila) |
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| Huvudupphovsmän: | , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2016
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4975549/ https://ncbi.nlm.nih.gov/pubmed/27488072 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/APO.0000000000000225 |
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