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Q33889479-FECD49B9-62FE-4120-BF19-0EC2E3717A9F
Q33889479-FECD49B9-62FE-4120-BF19-0EC2E3717A9F
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http://www.wikidata.org/entity/statement/Q33889479-FECD49B9-62FE-4120-BF19-0EC2E3717A9F
Whole-exome sequencing and its impact in hereditary hearing loss
P2860
Q33889479-FECD49B9-62FE-4120-BF19-0EC2E3717A9F
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http://www.wikidata.org/entity/statement/Q33889479-FECD49B9-62FE-4120-BF19-0EC2E3717A9F
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79550b5b848782230c616a59b040636422876c57
P2860
EPS8, encoding an actin-binding protein of cochlear hair cell stereocilia, is a new causal gene for autosomal recessive profound deafness.