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

<div>Schematic representation of the reported mutations in <i>MYO15A</i> and the corresponding protein structure. Mutations identified in this study were marked in red.</div>

Neural Plasticity

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Figure 4

Figure 4: Targeted Next-Generation Sequencing Identified Compound Heterozygous Mutations in <i>MYO15A</i> as the Probable Cause of Nonsyndromic Deafness in a Chinese Han Family 

Figure 4 | Targeted Next-Generation Sequencing Identified Compound Heterozygous Mutations in MYO15A as the Probable Cause of Nonsyndromic Deafness in a Chinese Han Family 