Autosomal dominant non-syndromic hearing loss caused by a novel mutation in MYO7A: A case report and review of the literature

Figure 1 Pedigree of the DFNA11 family. The arrow indicates the proband. Horizontal lines above the individuals indicate that genetic testing was performed. The age of each subject at the time of genetic testing is listed on the top-right region of each symbol. The genotype of MYO7A for each individual is indicated below the symbol, heterozygous mutant: c.1531G>A/- or wild type: -/-.