Cochlear Implantation in a Patient with a Novel POU3F4 Mutation and Incomplete Partition Type-III Malformation

Figure 1

Clinical phenotype presentations of the pedigree. (a) Pedigree of a Chinese family displaying X-linked inheritance hearing loss (arrow indicates the proband; mutation c.400_401insACTC in POU3F4 gene denoted as M); (b–d) Pure-tone audiograms of the family. Frequency in hertz (Hz) is plotted on the -axis and the hearing level in decibels (dB HL) on the -axis.

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