Compound Heterozygous Mutations in <i>TMC1</i> and <i>MYO15A</i> Are Associated with Autosomal Recessive Nonsyndromic Hearing Loss in Two Chinese Han Families

<div>(a) The Sanger sequencing results of the p.S3417del and p.R1407T mutations in <i>MYO15A</i> in Family 2. (b) Multispecies sequence alignment of the S3417 and R1407 residues.</div>

Neural Plasticity

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Figure 4

Figure 4: Compound Heterozygous Mutations in <i>TMC1</i> and <i>MYO15A</i> Are Associated with Autosomal Recessive Nonsyndromic Hearing Loss in Two Chinese Han Families 

Figure 4 | Compound Heterozygous Mutations in TMC1 and MYO15A Are Associated with Autosomal Recessive Nonsyndromic Hearing Loss in Two Chinese Han Families 