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Q33530552-A64361F4-6D1A-42D2-9123-A9C70C647474
Q33530552-A64361F4-6D1A-42D2-9123-A9C70C647474
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http://www.wikidata.org/entity/statement/Q33530552-A64361F4-6D1A-42D2-9123-A9C70C647474
High-throughput detection of mutations responsible for childhood hearing loss using resequencing microarrays.
P2860
Q33530552-A64361F4-6D1A-42D2-9123-A9C70C647474
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33530552-A64361F4-6D1A-42D2-9123-A9C70C647474
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7f47e9e980bfb9b7a732ec6b6f3adb7c5f0ad090
P2860
High frequency of the IVS2-2A>G DNA sequence variation in SLC26A5, encoding the cochlear motor protein prestin, precludes its involvement in hereditary hearing loss.