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  • Molecular assay reagents intended to identify mutations in the POU class 3 homeobox 4 (POU3F4) gene, located at chromosome Xq21.1, which encodes for a protein that helps regulate the activity of other genes (transcription factor). This genetic mutation has been identified in patients with X-linked nonsyndromic deafness type 3 (i.e., DFN3).
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