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Q30543886-3CF6EAAC-E4B0-431B-82BC-55A17A3FCEF5
Q30543886-3CF6EAAC-E4B0-431B-82BC-55A17A3FCEF5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30543886-3CF6EAAC-E4B0-431B-82BC-55A17A3FCEF5
Hereditary non-syndromic sensorineural hearing loss: transforming silence to sound
P2860
Q30543886-3CF6EAAC-E4B0-431B-82BC-55A17A3FCEF5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30543886-3CF6EAAC-E4B0-431B-82BC-55A17A3FCEF5
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wasDerivedFrom
a6bbe58ea2e2566cd55f80a590caca672234d6c3
P2860
Clinical phenotype and mutations in connexin 26 (DFNB1/GJB2), the most common cause of childhood hearing loss.