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2 | 15841390 | 2005 | Li, Z., Li, R., Chen, J., Liao, Z., Zhu, Y., Qian, Y., Xiong, S., Heman-Ackah, S., Wu, J., Choo, D. I., Guan, M. X. (2005) Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss Human Genetics . 117 (1): 9-15 . |
3 | 16528519 | 2006 | Yao, Y. G., Salas, A., Bravi, C. M., Bandelt, H. J. (2006) A reappraisal of complete mtDNA variation in East Asian families with hearing impairment Human Genetics . 119 (5): 505-515 . |
4 | 16650816 | 2006 | Xing, G., Chen, Z., Wei, Q., Tian, H., Li, X., Zhou, A., Bu, X., Cao, X. (2006) Maternally inherited non-syndromic hearing loss associated with mitochondrial 12S rRNA A827G mutation in a Chinese family Biochemical and Biophysical Research Communications . 344 (4): 1253-1257 . |
5 | 16782057 | 2006 | Xing, G., Chen, Z., Wei, Q., Tian, H., Li, X., Zhou, A., Bu, X., Cao, X. (2006) Mitochondrial 12S rRNA A827G mutation is involved in the genetic susceptibility to aminoglycoside ototoxicity Biochemical and Biophysical Research Communications . 346 (4): 1131-1135 . |
6 | 17489842 | 2007 | Kokotas, H., Petersen, M. B., Willems, P. J. (2007) Mitochondrial deafness Clinical Genetics . 71 (5): 379-391 . |
7 | 18261986 | 2008 | Chaig, M. R., Zernotti, M. E., Soria, N. W., Romero, O. F., Romero, M. F., Gerez, N. M. (2008) A mutation in mitochondrial 12S rRNA, A827G, in Argentinean family with hearing loss after aminoglycoside treatment Biochemical and Biophysical Research Communications . 368 (3): 631-636 . |
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10 | 19144107 | 2009 | Bardien, S., Human, H., Harris, T., Hefke, G., Veikondis, R., Schaaf, H. S., van der Merwe, L., Greinwald, J. H., Fagan, J., de Jong, G. (2009) A rapid method for detection of five known mutations associated with aminoglycoside-induced deafness BMC Medical Genetics . 10 (-): 2 . |
11 | 19371214 | 2009 | Rydzanicz, M., Wrobel, M., Cywinska, K., Froehlich, D., Gawecki, W., Szyfter, W., Szyfter, K. (2009) Screening of the general Polish population for deafness-associated mutations in mitochondrial 12S rRNA and tRNA Ser(UCN) genes Genetic Testing and Molecular Biomarkers . 13 (2): 167-172 . |
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13 | 20353758 | 2010 | Rydzanicz, M., Wrobel, M., Pollak, A., Gawecki, W., Brauze, D., Kostrzewska-Poczekaj, M., Wojsyk-Banaszak, I., Lechowicz, U., Mueller-Malesinska, M., Oldak, M., Ploski, R., Skarzynski, H., Szyfter, K. (2010) Mutation analysis of mitochondrial 12S rRNA gene in Polish patients with non-syndromic and aminoglycoside-induced hearing loss Biochemical and Biophysical Research Communications . 395 (1): 116-121 . |
14 | 20722495 | 2010 | Uehara, D. T., Rincon, D., Abreu-Silva, R. S., Auricchio, M. T., Tabith, A., Kok, F., Mingroni-Netto, R. C. (2010) Role of the mitochondrial mutations, m.827A>G and the novel m.7462C>T, in the origin of hearing loss Genetic Testing and Molecular Biomarkers . 14 (5): 611-616 . |
15 | 21495045 | 2011 | Ealy, M., Lynch, K. A., Meyer, N. C., Smith, R. J. (2011) The prevalence of mitochondrial mutations associated with aminoglycoside-induced sensorineural hearing loss in an NICU population Laryngoscope . 121 (6): 1184-1186 . |
16 | 27230773 | 2016 | Alves, R. M., da Silva Costa, S. M., do Amor Divino Miranda, P. M., Ramos, P. Z., Marconi, T. G., Santos Oliveira, G., Castilho, A. M., Sartorato, E. L. (2016) Analysis of mitochondrial alterations in Brazilian patients with sensorineural hearing loss using MALDI-TOF mass spectrometry BMC Medical Genetics . 17 (1): 41 . |
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