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GNB1-Related Rod-Cone Dystrophy: A Case Report
Download from doi.orgLoss-of-function variants in UBAP1L cause autosomal recessive retinal degeneration
UploadGenetic profile of syndromic retinitis pigmentosa in Portugal
UploadTBC1D32 variants disrupt retinal ciliogenesis and cause retinitis pigmentosa
Download from doi.orgA Unique Presentation of Bilateral Chorioretinal Atrophy
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