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Homozygous Variant in ARL3 Causes Autosomal Recessive Cone Rod Dystrophy
PURPOSE: Cone rod dystrophy (CRD) is a group of inherited retinopathies characterized by the loss of cone and rod photoreceptor cells, which results in poor vision. This study aims to clinically and genetically characterize the segregating CRD phenotype in two large, consanguineous Pakistani familie...
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| Pubblicato in: | Invest Ophthalmol Vis Sci |
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| Autori principali: | , , , , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
The Association for Research in Vision and Ophthalmology
2019
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6944245/ https://ncbi.nlm.nih.gov/pubmed/31743939 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.19-27263 |
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