Autosomal Recessive Congenital Sensorineural Hearing Loss due to a Novel Compound Heterozygous PTPRQ Mutation in a Chinese Family

<div>Pedigree of the affected Family 1 with congenital SNHL. Sanger sequencing analysis showed that patient II1 had the compound heterozygous mutation (c.[1973T&gt;C]; c.[4472C&gt;T]), and the parents and sister had the heterozygous mutation. The patient is denoted in black. [=] means wild type.</div>

Neural Plasticity

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Figure 1

Figure 1: Autosomal Recessive Congenital Sensorineural Hearing Loss due to a Novel Compound Heterozygous PTPRQ Mutation in a Chinese Family 