MITOMAP References for Mutation G-A at 9804

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Index PMID Date Reference
1 8240356 1993 Johns, D. R., Neufeld, M. J. (1993) Cytochrome c oxidase mutations in Leber hereditary optic neuropathy Biochemical and Biophysical Research Communications . 196 (2): 810-815 .
2 7599218 1995 Savontaus, M.L. (1995) mtDNA mutations in Leber's hereditary optic neuropathy Biochimica et Biophysica Acta . 1271 (1): 261-263 .
3 7710535 1995 Newman, N.J., Torroni, A., Brown, M.D., Lott, M.T., Wallace, D.C., Philen, R., Roman, G.C. (1995) Cuban optic neuropathy [letter; comment] Neurology . 45 (2): 397 .
4 10520236 1999 Matsumoto, M., Hayasaka, S., Kadoi, C., Hotta, Y., Fujiki, K., Fujimaki, T., Takeda, M., Ishida, N., Endo, S., Kanai, A. (1999) Secondary mutations of mitochondrial DNA in Japanese patients with Leber's hereditary optic neuropathy Ophthalmic Genetics . 20 (3): 153-160 .
5 11339587 2001 Dogulu, C. F., Kansu, T., Seyrantepe, V., Ozguc, M., Topaloglu, H., Johns, D. R. (2001) Mitochondrial DNA analysis in the Turkish Leber's hereditary optic neuropathy population Eye (London) . 15 (Pt 2): 183-188 .
6 11579587 2001 Yamada, K., Mashima, Y., Hiida, Y., Oguchi, Y. (2001) [DNA diagnosis of Leber's hereditary optic neuropathy performed at Keio University Hospital] Nippon Ganka Gakkai Zasshi . 105 (9): 608-613 .
7 16132471 2005 de Magalhaes, J. P. (2005) Human disease-associated mitochondrial mutations fixed in nonhuman primates Journal of Molecular Evolution . 61 (4): 491-497 .
8 21457906 2011 Pereira, L., Soares, P., Radivojac, P., Li, B., Samuels, D. C. (2011) Comparing phylogeny and the predicted pathogenicity of protein variations reveals equal purifying selection across the global human mtDNA diversity American Journal of Human Genetics . 88 (4): 433-439 .
9 NA 2014 van Oven, M., Kayser, M. (2014) . http://www.phylotree.org . Variants appear in tree, sequence(s) available. Phylotree (Build 16): 19 Feb .
10 23735083 2014 Tansel, T., Pacal, F., Ustek, D. (2014) A novel ATP8 gene mutation in an infant with tetralogy of Fallot Cardiology in the Young . 24 (3): 531-533 .
11 27119776 2016 Souren, N. Y., Gerdes, L. A., Kumpfel, T., Lutsik, P., Klopstock, T., Hohlfeld, R., Walter, J. (2016) Mitochondrial DNA variation and heteroplasmy in monozygotic twins clinically discordant for multiple sclerosis Human Mutation . 37 (8): 765-775 .
12 30831606 2019 Lazdinyte, S., Schorderet, D. F., Schaller, A., Valmaggia, C., Todorova, M. G. (2019) Analysis of inherited optic neuropathies Klinische Monatsblatter fur Augenheilkunde . 236 (4): 451-461 .