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Unique haplotype in exon 3 of cone opsin mRNA affects splicing of its precursor, leading to congenital color vision defect

Unique HaplotypeDevelopmental BiologyGenetic DisorderNatural SciencesGeneticsGenomic MechanismMolecular BiologyCone Opsin MrnaExon 3Molecular GeneticsDisease Gene IdentificationGene ExpressionMedicineSplicing Variant