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A Carrier Female Manifesting an Unusual X-Linked Retinoschisis Phenotype Associated with the Pathogenic Variant c.266delA, p.(Tyr89LeufsTer37) in RS1, and Skewed X-Inactivation
 
 
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Genes 2023, 14(7), 1438; https://doi.org/10.3390/genes14071438
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