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Genotype determination of the OPN1LW/OPN1MW genes: novel disease-causing mechanisms in Japanese patients with blue cone monochromacy | Scientific Reports
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The landscape of submicroscopic structural variants at the OPN1LW/OPN1MW gene cluster on Xq28 underlying blue cone monochromacy | PNAS
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IJMS | Free Full-Text | Novel OPN1LW/OPN1MW Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone Dysfunction
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Genotype determination of the OPN1LW/OPN1MW genes: novel disease-causing mechanisms in Japanese patients with blue cone monochromacy | Scientific Reports
Intermixing the OPN1LW and OPN1MW Genes Disrupts the Exonic Splicing Code Causing an Array of Vision Disorders
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Genotype determination of the OPN1LW/OPN1MW genes: novel disease-causing mechanisms in Japanese patients with blue cone monochromacy | Scientific Reports
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Diagram of the ;5.5 kb of the OPN1LW gene region analyzed in humans... | Download Scientific Diagram
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Diagram of the ;5.5 kb of the OPN1LW gene region analyzed in humans... | Download Scientific Diagram
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Novel OPN1LW/OPN1MW deletion mutations in 2 Japanese families with blue cone monochromacy | Human Genome Variation
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Mutation and opsin gene arrays in mother and son. (A) Sequence data... | Download Scientific Diagram
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Schematic comparing the nucleotide sequences and amino acid profile of... | Download Scientific Diagram
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