MITOMAP References for RNA Mutation T961G

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Index PMID Date Reference
1 15286157 2004 Li, R., Greinwald, J. H., Jr., Yang, L., Choo, D. I., Wenstrup, R. J., Guan, M. X. (2004) Molecular analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in paediatric subjects with non-syndromic hearing loss Journal of Medical Genetics . 41 (8): 615-620 .
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 19705751 2009 Dzhemileva, L. U., Posukh, O. L., Tazetdinov, A. M., Barashkov, N. A., Zhuravskii, S. G., Ponidelko, S. N., Markova, T. G., Tadinova, V. N., Fedorova, S. A., Maksimova, N. R., Khusnutdinova, E. K. (2009) [Analysis of mitochondrial 12S rRNA and tRNA(Ser(UCN)) genes in patients with nonsyndromic sensorineural hearing loss from various regions of Russia] Genetika . 45 (7): 982-991 .
4 23013294 2012 Turchetta, R., Mazzei, F., Celani, T., Cammeresi, M. G., Orlando, M. P., Altissimi, G., de Vincentiis, C., D'Ambrosio, F., Messineo, D., Ferraris, A., Cianfrone, G. (2012) Audiological and radiological characteristics of a family with T961G mitochondrial mutation International Journal of Audiology . 51 (12): 870-879 .
5 23969527 2013 Guaran, V., Astolfi, L., Castiglione, A., Simoni, E., Olivetto, E., Galasso, M., Trevisi, P., Busi, M., Volinia, S., Martini, A. (2013) Association between idiopathic hearing loss and mitochondrial DNA mutations: a study on 169 hearing-impaired subjects International Journal of Molecular Medicine . 32 (4): 785-794 .
6 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 .
7 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 .