Neural Plasticity / 2020 / Article / Fig 4

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 4

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

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