Genetics Research International / 2011 / Article / Fig 2

Research Article

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.
(a) wild type
(b) Homozyous Deletion
(c) Heterozygous Carrier

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