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Genomic DNA nanoparticles rescue rhodopsin-associated retinitis pigmentosa phenotype
Mutations in the rhodopsin gene cause retinal degeneration and clinical phenotypes including retinitis pigmentosa (RP) and congenital stationary night blindness. Effective gene therapies have been difficult to develop, however, because generating precise levels of rhodopsin expression is critical; o...
Tallennettuna:
| Julkaisussa: | FASEB J |
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| Päätekijät: | , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Federation of American Societies for Experimental Biology
2015
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4447225/ https://ncbi.nlm.nih.gov/pubmed/25713057 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1096/fj.15-270363 |
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