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  • Molecular assay reagents intended to identify mutations in the PRP8 pre-mRNA processing factor 8 homologue (S. cerevisiae) gene, located at chromosome 17p13.3, which encodes for a protein that is essential for the catalytic step in pre-mRNA splicing process. This genetic mutation has been identified in patients with retinitis pigmentosa type 13 (RP13).
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