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.R34X and p.M413T mutations in <i>TMC1</i> in Family 1. (b) Multispecies sequence alignment of the M413 residue.</div>

Neural Plasticity

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Figure 3: 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 3 | Compound Heterozygous Mutations in TMC1 and MYO15A Are Associated with Autosomal Recessive Nonsyndromic Hearing Loss in Two Chinese Han Families 