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  • Molecular assay reagents intended to identify mutations in the cone-rod homeobox (CRX) gene, located at chromosome 19q13.3, which encodes for a protein that is a photoreceptor-specific transcription factor involved in the differentiation of photoreceptor cells. Mutations at this locus have been identified in patients with Leber\'s congenital amaurosis and cone-rod dystrophy 2 (CORD2).
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