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2. C1494T mitochondrial DNA mutation, hearing loss, and aminoglycosides antibiotics. Postal M; Palodeto B; Sartorato EL; Oliveira CA Braz J Otorhinolaryngol; 2009; 75(6):884-7. PubMed ID: 20209292 [TBL] [Abstract][Full Text] [Related]
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11. The frequency in New Zealand of a mitochondrial DNA mutation (1555 A to G) associated with aminoglycoside-induced hearing loss. Scrimshaw BJ; Faed JM; Tate WP; Yun K N Z Med J; 1999 Jun; 112(1089):216-7. PubMed ID: 10414625 [No Abstract] [Full Text] [Related]
12. Reply: Both mitochondrial DNA and mitonuclear gene mutations cause hearing loss through cochlear dysfunction. Santarelli R; Cama E; Scimemi P; La Morgia C; Caporali L; Valentino ML; Liguori R; Carelli V Brain; 2016 Jun; 139(Pt 6):e34. PubMed ID: 27016406 [No Abstract] [Full Text] [Related]
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20. Prevalence of mitochondrial gene mutations among hearing impaired patients. Usami S; Abe S; Akita J; Namba A; Shinkawa H; Ishii M; Iwasaki S; Hoshino T; Ito J; Doi K; Kubo T; Nakagawa T; Komiyama S; Tono T; Komune S J Med Genet; 2000 Jan; 37(1):38-40. PubMed ID: 10633132 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]