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An autosomal dominant retinopathy caused by variants in the RP1 gene.
No clinical trials have been registered for RP1-related recessive retinopathy.
4 publications have been identified in PubMed for RP1-related recessive retinopathy. Research spans Other (25%), Case Report / Case Series (25%), and Basic Science / Preclinical (25%).
Chiu HI (2025). [PMID: 40335823](https://pubmed.ncbi.nlm.nih.gov/40335823/). *Ophthalmol Ther*. [Other]
Choi SW (2024). [PMID: 39087930](https://pubmed.ncbi.nlm.nih.gov/39087930/). *Transl Vis Sci Technol*. [Case Report / Case Series]
Dimopoulos IS (2024). [PMID: 38478753](https://pubmed.ncbi.nlm.nih.gov/38478753/). *Retina*. [Basic Science / Preclinical]
Natsume K (2024). [PMID: 39463394](https://pubmed.ncbi.nlm.nih.gov/39463394/). *Sci Rep*. [Epidemiology / Natural History]
Data assembled from 2 of 12 sources · Last updated Sep 20, 2026, 1:50 AM UTC
Common questions about RP1-related recessive retinopathy