Research Article

Targeted Next-Generation Sequencing Identified Compound Heterozygous Mutations in MYO15A as the Probable Cause of Nonsyndromic Deafness in a Chinese Han Family

Figure 2

(a) Audiogram of the proband (II-1) before and after cochlear implantation and that of his unaffected sister (II-2). (b) Temporal bone Computerized Tomography (CT) scan of the proband (II-1). (c) Cranial Magnetic Resonance Imaging (MRI) of the proband (II-1).
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