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TMC1 but not TMC2 is responsible for autosomal recessive nonsyndromic hearing impairment in Tunisian families
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Amino acid 572 in TMC1: hot spot or critical functional residue for dominant mutations causing hearing impairment
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A novel mutation at the DFNA36 hearing loss locus reveals a critical function and potential genotype-phenotype correlation for amino acid-572 of TMC1
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TMC and EVER genes belong to a larger novel family, the TMC gene family encoding transmembrane proteins
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