Identification of Novel Compound Heterozygous <i>MYO15A</i> Mutations in Two Chinese Families with Autosomal Recessive Nonsyndromic Hearing Loss

<div>(a) Schematic diagram of 66 exons of the <i>MYO15A</i> gene is shown with all pathogenic mutations (arrows) of two families. Novel compound heterozygous <i>MYO15A</i> mutations are indicated in red. Previously reported mutation is indicated in black. (b) Overview of the reported <i>MYO15A</i> variants and their locations in the protein structure. The red words indicate the novel mutations, and the blue one refers to the reported variant that was detected in the proband in this study.</div>

Neural Plasticity

fig3

Figure 3

Figure 3: Identification of Novel Compound Heterozygous <i>MYO15A</i> Mutations in Two Chinese Families with Autosomal Recessive Nonsyndromic Hearing Loss 

Neural Plasticity

Identification of Novel Compound Heterozygous MYO15A Mutations in Two Chinese Families with Autosomal Recessive Nonsyndromic Hearing Loss

Figure 3