Prevalence of Retinitis Pigmentosa in Maine

Retinitis pigmentosa

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A point mutation of the rhodopsin gene in one form of retinitis pigmentosa

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Non-syndromic retinitis pigmentosa

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A Null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa

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Worldwide carrier frequency and genetic prevalence of autosomal recessive inherited retinal diseases

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First-in-human trial of a novel suprachoroidal retinal prosthesis

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Photoreceptor cell rescue in retinal degeneration (rd) mice by in vivo gene therapy

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Retinitis pigmentosa and allied diseases: numerous diseases, genes, and inheritance patterns

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Accelerated Accumulation of Lipofuscin Pigments in the RPE of a Mouse Model for ABCA4-Mediated Retinal Dystrophies following Vitamin A Supplementation

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Predicting visual sensitivity in retinal prosthesis patients

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ω-3 Intake and Visual Acuity in Patients With Retinitis Pigmentosa Receiving Vitamin A

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Nr2e3 is a genetic modifier that rescues retinal degeneration and promotes homeostasis in multiple models of retinitis pigmentosa

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pulse2percept: A Python-based simulation framework for bionic vision

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Temporal interactions during paired-electrode stimulation in two retinal prosthesis subjects

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Development of very large electrode arrays for epiretinal stimulation (VLARS)

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Syndromic retinitis pigmentosa.

Karuntu, J. S., Almushattat, H., Nguyen, X.-T.-A., Plomp, A. S., Wanders, R. J. A., Hoyng, C. B., van Schooneveld, M. J., Schalij-Delfos, N. E., Brands, M. M., Leroy, B. P., et al. (2025) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2024.101324 · Cited by 39

A homozygous p.Glu150Lys mutation in the opsin gene of two Pakistani families with autosomal recessive retinitis pigmentosa.

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Mapping X-linked Ophthalmic Diseases: III. Provisional Assignment of the Locus for Blue Cone Monochromacy to Xq28

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Genetic Analysis of the Rhodopsin Gene Identifies a Mosaic Dominant Retinitis Pigmentosa Mutation in a Healthy Individual

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A novel LRAT mutation affecting splicing in a family with early onset retinitis pigmentosa

Chen, Y., Huang, L., Jiao, X., Riazuddin, S., Riazuddin, S. A., & Fielding Hetmancik, J. (2018) · Human Genomics · doi:10.1186/s40246-018-0165-3 · Cited by 18