Research Article

Three MYO15A Mutations Identified in One Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss

Figure 1

Clinical phenotype presentations of the pedigree. (a) Disease presentation of the family members and the pedigree map. All living members participated in the study, and V-3, V-4, and IV-2 were sequenced using capture gene sequencing. (b) Pure-tone audiograms of the family. Frequency in hertz (Hz) is plotted on the x-axis and the hearing level in decibels (dBHL) on the y-axis. The arrows in blue or red mean that the pure tones are not elicited at this point.
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