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Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense...
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Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is cause...
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Characterization of a new full length TMPRSS3 isoform and identification of muta...
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Characterization of a new full length TMPRSS3 isoform and identification of muta...
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Characterization of a new full length TMPRSS3 isoform and identification of muta...
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Characterization of a new full length TMPRSS3isoform and identification of mutan...
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Characterization of a new full length TMPRSS3 isoform and identification of muta...
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