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Mutation Discovered in a Feline Model of Human Congenital Retinal Blinding Disease
PURPOSE. To elucidate the gene defect in a pedigree of cats segregating for autosomal dominant rod–cone dysplasia (Rdy), a retinopathy characterized extensively from a clinical perspective. Disease expression in Rdy cats is comparable to that in young patients with congenital blindness (Leber congen...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Association for Research in Vision and Ophthalmology, Inc.
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2891453/ https://ncbi.nlm.nih.gov/pubmed/20053974 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.09-4261 |
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