Neural Plasticity / 2020 / Article / Fig 3

Research Article

Targeted Next-Generation Sequencing Identified Compound Heterozygous Mutations in MYO15A as the Probable Cause of Nonsyndromic Deafness in a Chinese Han Family

Figure 3

Sanger sequencing results of the c.3658_3662del and c.6177+1G>T mutations in the family members.
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