Literature DB >> 10414625

The frequency in New Zealand of a mitochondrial DNA mutation (1555 A to G) associated with aminoglycoside-induced hearing loss.

B J Scrimshaw, J M Faed, W P Tate, K Yun.   

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Year:  1999        PMID： 10414625

Source DB:  PubMed          Journal:  N Z Med J        ISSN： 0028-8446


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  1 in total

1.  The prevalence of mitochondrial mutations associated with aminoglycoside-induced deafness in ethnic Latvian population: the appraisal of the evidence.

Authors:  Viktorija Igumnova; Lauma Veidemane; Anda Vīksna; Valentina Capligina; Egija Zole; Renate Ranka
Journal:  J Hum Genet       Date:  2018-12-06       Impact factor: 3.172
  1 in total

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