MITOMAP References for RNA Mutation C960CC

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Index PMID Date Reference
1 12394346 2002 Tang, H. Y., Hutcheson, E., Neill, S., Drummond-Borg, M., Speer, M., Alford, R. L. (2002) Genetic susceptibility to aminoglycoside ototoxicity: how many are at risk? Genetics in Medicine . 4 (5): 336-345 .
2 18851951 2008 Elstner, M., Schmidt, C., Zingler, V. C., Prokisch, H., Bettecken, T., Elson, J. L., Rudolph, G., Bender, A., Halmagyi, G. M., Brandt, T., Strupp, M., Klopstock, T. (2008) Mitochondrial 12S rRNA susceptibility mutations in aminoglycoside-associated and idiopathic bilateral vestibulopathy Biochemical and Biophysical Research Communications . 377 (2): 379-383 .
3 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 .
4 27654872 2016 Barbarino, J. M., McGregor, T. L., Altman, R. B., Klein, T. E. (2016) PharmGKB summary: very important pharmacogene information for MT-RNR1 Pharmacogenetics and Genomics . 26 (12): 558-567 .
5 30523288 2019 Igumnova, V., Veidemane, L., Viksna, A., Capligina, V., Zole, E., Ranka, R. (2019) The prevalence of mitochondrial mutations associated with aminoglycoside-induced deafness in ethnic Latvian population: the appraisal of the evidence Journal of Human Genetics . 64 (3): 199-206 .