Research Article
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
Figure 1
Pedigree of the family and clinical findings of the proband IV-1: (a) pedigree and genotype showing the c.481C>T (p.R161C) mutation in SOX10 and the c.235delC (p.L79Cfs3) mutation in GJB2; (b) auditory evoked potentials showing bilateral profound sensorineural hearing loss.
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