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

<div>Protein molecular models of wild types and PTPRQ mutations. (a) The mutation protein M1491 has a different side chain to the wild-type protein T1491. (b) The wild-type protein has a longer side chain than the mutation protein A658.</div>

Neural Plasticity

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Figure 3

Figure 3: Autosomal Recessive Congenital Sensorineural Hearing Loss due to a Novel Compound Heterozygous PTPRQ Mutation in a Chinese Family 