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Gene Therapy in the Retinal Degeneration Slow Model of Retinitis Pigmentosa
Human blinding disorders are often initiated by hereditary mutations that insult rod and/or cone photoreceptors and cause subsequent cellular death. Generally, the disease phenotype can be predicted from the specific mutation as many photoreceptor genes are specific to rods or cones; however certain...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3161507/ https://ncbi.nlm.nih.gov/pubmed/20238065 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/978-1-4419-1399-9_70 |
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