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ATF6 Is Mutated in Early Onset Photoreceptor Degeneration With Macular Involvement
PURPOSE. Photoreceptor degeneration (PRD) is a genetically heterogeneous retinal disorder. Although a number of genes involved in PRD have been identified, their genetic basis remains unknown in a significant number of patients. In this study, we aimed to identify novel disease-causing genes of PRD....
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| Gepubliceerd in: | Invest Ophthalmol Vis Sci |
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| Hoofdauteurs: | , , , , , , , , , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
The Association for Research in Vision and Ophthalmology
2015
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4468593/ https://ncbi.nlm.nih.gov/pubmed/26070061 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.15-16778 |
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