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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Natural History of PRPF31 Mutation-Associated Retinal DystrophyCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, eye disorder, hereditary disease, inherited retinal dystrophy, retinal degeneration, retinal disorder, retinitis pigmentosaActive, not recruitingNot stated2026-04-13NCT05573984