Literature DB >> 9950117

Aminoglycoside-induced deafness associated with the mitochondrial DNA mutation A1555G.

M Shohat1, N Fischel-Ghodsian, C Legum, G J Halpern.   

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Year:  1999        PMID： 9950117     DOI： 10.1016/s0196-0709(99)90054-6

Source DB:  PubMed          Journal:  Am J Otolaryngol        ISSN： 0196-0709            Impact factor:   1.808


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  2 in total

1.  Elucidation of separate, but collaborative functions of the rRNA methyltransferase-related human mitochondrial transcription factors B1 and B2 in mitochondrial biogenesis reveals new insight into maternally inherited deafness.

Authors:  Justin Cotney; Sharen E McKay; Gerald S Shadel
Journal:  Hum Mol Genet       Date:  2009-05-05       Impact factor: 6.150

Review 2.  PharmGKB summary: very important pharmacogene information for MT-RNR1.

Authors:  Julia M Barbarino; Tracy L McGregor; Russ B Altman; Teri E Klein
Journal:  Pharmacogenet Genomics       Date:  2016-12       Impact factor: 2.089
  2 in total

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