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Q24791654-01BF737E-3910-41B8-BBF1-4987A68D79F3
Q24791654-01BF737E-3910-41B8-BBF1-4987A68D79F3
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http://www.wikidata.org/entity/statement/Q24791654-01BF737E-3910-41B8-BBF1-4987A68D79F3
Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss
P2860
Q24791654-01BF737E-3910-41B8-BBF1-4987A68D79F3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24791654-01BF737E-3910-41B8-BBF1-4987A68D79F3
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wasDerivedFrom
46586fd5da8cdc279bca4ed8f8335ef71d7a1afe
P2860
Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction.