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X-linked Retinoschisis — Gene Therapy & Clinical Trials | FollowGene

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Home/Diseases/X-linked Retinoschisis

X-linked Retinoschisis

Prevalence: 1/15000

ophthalmologic

Official·OMIM:312700 Official·ORPHA792

Retinal layer splitting due to RS1 gene mutations.

Associated Genes

RS1Retinoschisin 1

Chromosome XX-Linked Recessive

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