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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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USH3A transcripts encode clarin-1, a four- transmembrane-domain protein with a possible role in sensory synapses
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Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC
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A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C
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