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Q50453175-E0DF2583-F6F5-4D6E-9498-790442AF8304
Q50453175-E0DF2583-F6F5-4D6E-9498-790442AF8304
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http://www.wikidata.org/entity/statement/Q50453175-E0DF2583-F6F5-4D6E-9498-790442AF8304
A maternal hereditary deafness pedigree of the A1555G mitochondrial mutation, causing aminoglycoside ototoxicity predisposition.
P2860
Q50453175-E0DF2583-F6F5-4D6E-9498-790442AF8304
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50453175-E0DF2583-F6F5-4D6E-9498-790442AF8304
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wasDerivedFrom
8481b5114e38341d5f0d5ab2af25e8c2878a82f1
P2860
Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss