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PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23
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Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31
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CDH23 mutation and phenotype heterogeneity:: A profile of 107 diverse families with Usher syndrome and nonsyndromic deafness
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Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D
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