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Soluble CX3CL1 gene therapy improves cone survival and function in mouse models of retinitis pigmentosa
Retinitis pigmentosa (RP) is a disease that initially presents as night blindness due to genetic deficits in the rod photoreceptors of the retina. Rods then die, causing dysfunction and death of cone photoreceptors, the cell type that mediates high acuity and color vision, ultimately leading to blin...
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| Publicado no: | Proc Natl Acad Sci U S A |
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| Principais autores: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
National Academy of Sciences
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6525490/ https://ncbi.nlm.nih.gov/pubmed/31036641 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1901787116 |
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