Targeted Next-Generation Sequencing Identifies Separate Causes of Hearing Loss in One Deaf Family and Variable Clinical Manifestations for the p.R161C Mutation in <i>SOX10</i>

<div>Schematic representation of the SOX10 domains and overview of <i>SOX10</i> mutations and their associated phenotypes.</div>

Neural Plasticity

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Figure 3

Figure 3: Targeted Next-Generation Sequencing Identifies Separate Causes of Hearing Loss in One Deaf Family and Variable Clinical Manifestations for the p.R161C Mutation in <i>SOX10</i> 

Figure 3 | Targeted Next-Generation Sequencing Identifies Separate Causes of Hearing Loss in One Deaf Family and Variable Clinical Manifestations for the p.R161C Mutation in SOX10 