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) Transmembrane domain structure of TMC1 and mutations in the second extracellular loop of <i>TMC1</i>. The novel p.M413T mutation identified in this study is in red. (b) Protein structure of Myosin XVA and missense mutations in the motor domain. The novel p.R1407T mutation identified in this study is in red.</div>

Neural Plasticity

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Figure 5

Figure 5: 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 5 | Compound Heterozygous Mutations in TMC1 and MYO15A Are Associated with Autosomal Recessive Nonsyndromic Hearing Loss in Two Chinese Han Families 