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  1. TRMU Deficiency - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK591557
    ... G (a variant known to be associated with aminoglycoside-induced deafness). This modifier ... Diagnosis The differential diagnosis of TRMU deficiency includes Leigh ...
  2. Nonsyndromic hearing loss 
    https://medlineplus.gov/genetics/condition/nonsyndromic-hearing-loss
    ... ClinicalTrials.gov DEAFNESS, AUTOSOMAL DOMINANT 7; DFNA7 DEAFNESS, AMINOGLYCOSIDE-INDUCED DEAFNESS, AUTOSOMAL RECESSIVE 2; DFNB2 DEAFNESS, AUTOSOMAL DOMINANT 4A; ...
  3. Nonsyndromic Hearing Loss and Deafness, Mitochondrial - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1422
    ... 1494C>T pathogenic variant was 31.7% when aminoglycoside-induced deafness was included and 17.5% when it was ... for detection of five known mutations associated with aminoglycoside-induced deafness. BMC Med Genet. 2009; 10 :2. [ PMC free ...
  4. Genetic Hearing Loss Overview - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1434
    ... to Family Members See Nonsyndromic Hearing Loss and Deafness, Mitochondrial for genetic counseling information about maternal inheritance. Empiric Risk to Family Members If a specific diagnosis cannot be established (and/or the mode of ...
  5. NLM Digital Collections - Hospital literature index (Volume 47) 
    resource.nlm.nih.gov/7807587X34
    ... 6-19 (20 ref.) Drug usage evaluation of aminoglycoside-induced nephrotoxicity in a community hospital. Wade WE, et ... 26(2): 132-6 Drug usage evaluation of aminoglycoside-induced nephrotoxicity in a community hospital. Wade WE, et ...