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Q24791654-1157693E-49F7-4A9D-8657-A742B785A0DE
Q24791654-1157693E-49F7-4A9D-8657-A742B785A0DE
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http://www.wikidata.org/entity/statement/Q24791654-1157693E-49F7-4A9D-8657-A742B785A0DE
Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss
P2860
Q24791654-1157693E-49F7-4A9D-8657-A742B785A0DE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24791654-1157693E-49F7-4A9D-8657-A742B785A0DE
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wasDerivedFrom
46586fd5da8cdc279bca4ed8f8335ef71d7a1afe
P2860
Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation.