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7 results
  1. 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 ...
  2. Nonsyndromic hearing loss: MedlinePlus Genetics 
    https://medlineplus.gov/genetics/condition/nonsyndromic-hearing-loss
    ... from OMIM DEAFNESS, AUTOSOMAL DOMINANT 7; DFNA7 DEAFNESS, AMINOGLYCOSIDE-INDUCED DEAFNESS, AUTOSOMAL RECESSIVE 2; DFNB2 DEAFNESS, AUTOSOMAL DOMINANT 4A; ...
  3. Mitochondrial Disorders Overview - GeneReviews® - NCBI Bookshelf 
    https://www.ncbi.nlm.nih.gov/books/NBK1224
    ... sensorineural deafness (m.7445A>G) rRNA genes 1 Aminoglycoside-induced nonsyndromic deafness (m.1555A>G) For the genetic code, gene ... with maternally transmitted type II diabetes mellitus and deafness. Nat Genet. ... counseling and prenatal diagnosis for the mitochondrial DNA mutations at nucleotide 8993. ...
  4. 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 ...