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rod cone
Summary
General Info
Curated Studies
Most Correlated Studies
OMIM - Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma
OMIM - Retinal dystrophy
OMIM - Spondylometaphyseal dysplasia
OMIM - Progressive cone-rod dystrophy
Mouse Phenotypes - Unspecified hereditary retinal dystrophies
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Literature
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NPHP1 FULL DELETION CAUSES NEPHRONOPHTHISIS AND A CONE-ROD DYSTROPHY.
Progressive Cone-Rod Dystrophy and RPE Dysfunction in Mitfmi/+ Mice.
Clinical and Genetic Analysis of RDH12-Associated Retinopathy in 27 Chinese Families: A Hypomorphic …
Identification of a novel RPGR mutation associated with X-linked cone-rod dystrophy in a Chinese fam…
Retrospective Natural History Study of RPGR-Related Cone- and Cone-Rod Dystrophies While Expanding t…
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Clinical Trials
Most Relevant Clinical Trials
Rod and Cone Mediated Function in Retinal Disease
Promising ROd-cone DYstrophy Gene therapY
Interferon Gamma-1b Administered Topically for Macular Edema/Intraretinal Schisis Cysts in Rod-Cone …
Rod Sensitivity in Age-related Macular Degeneration (AMD) and Retinitis Pigmentosa (RP)
Study of New Mutations in Cone Disorders
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