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Q24815450-23CC618F-A605-455E-8CEB-91357DD5BEF5
Q24815450-23CC618F-A605-455E-8CEB-91357DD5BEF5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24815450-23CC618F-A605-455E-8CEB-91357DD5BEF5
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.
P2860
Q24815450-23CC618F-A605-455E-8CEB-91357DD5BEF5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24815450-23CC618F-A605-455E-8CEB-91357DD5BEF5
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type
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wasDerivedFrom
1eaf9ae92066c18ca4776a288ccdfaae73f4a96a
P2860
Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss