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G Mutation in European Children
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G is dramatic. Carriers of this mutation have permanent, profound hearing loss after receiving aminoglycosides, even when drug levels are within the therapeutic range.1,2 A review of previous studies indicates that after aminoglycoside exposure, penetrance of deafness in this population is close to 100%.3
Estimates of the prevalence of the m.1555A
G mutation have been hampered because of the small numbers of patients in such
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