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Figure 1 | Journal of Translational Medicine

Figure 1

From: Novel compound heterozygous mutations in the MYO15A gene in autosomal recessive hearing loss identified by whole-exome sequencing

Figure 1

Combined figure. A. Pedigree of Family 4792 with ARNSHL Affected subjects are denoted in black. Arrow indicates the proband; B. Audiogram of affected subjects showed hearing loss ranged from severe to profound.; C. Electropherograms analysis of MYO15A in family 4792 showing the compound heterozygous mutations (c.IVS25 + 3G > A and c.8375C > T) co-segregated with the phenotype.

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