Autosomal Recessive Nonsyndromic Hearing Impairment due to a Novel Deletion in the RDX Gene
Figure 2
Chromatogram displaying the novel RDX deletion c.1076_1079delTTAA (p.Ile359Lysfs*6). Chromatograms shown are from sequences of the following: (a) wild type, (b) hearing-impaired homozygous individual VII-1, and (c) unaffected heterozygous individual VI-5. The deleted nucleotides TTAA are indicated with a red triangle.
