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Residual Foveal Cone Structure in CNGB3-Associated Achromatopsia
PURPOSE: Congenital achromatopsia (ACHM) is an autosomal recessive disorder in which cone function is absent or severely reduced. Gene therapy in animal models of ACHM have shown restoration of cone function, though translation of these results to humans relies, in part, on the presence of viable co...
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| Publicado en: | Invest Ophthalmol Vis Sci |
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| Autores principales: | , , , , , , , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
The Association for Research in Vision and Ophthalmology
2016
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4978151/ https://ncbi.nlm.nih.gov/pubmed/27479814 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.16-19313 |
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