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GKI262
GKI262
http://dx.doi.org/10.1093/NAR/GKI262
Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss
P356
Q24791654-ACD6100D-1AD8-44F2-B8C9-EF86FE92780E
P356
GKI262
http://dx.doi.org/10.1093/NAR/GKI262