MITOMAP References for Mutation G-A at 3635

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1 11479733 2001 Brown, M. D., Zhadanov, S., Allen, J. C., Hosseini, S., Newman, N. J., Atamonov, V. V., Mikhailovskaya, I. E., Sukernik, R. I., Wallace, D. C. (2001) Novel mtDNA mutations and oxidative phosphorylation dysfunction in Russion LHON families Human Genetics . 109 (1): 33-39 .
2 25194554 2014 Zhang, J., Jiang, P., Jin, X., Liu, X., Zhang, M., Xie, S., Gao, M., Zhang, S., Sun, Y. H., Zhu, J., Ji, Y., Wei, Q. P., Tong, Y., Guan, M. X. (2014) Leber's hereditary optic neuropathy caused by the homoplasmic ND1 m.3635G>A mutation in nine Han Chinese families Mitochondrion . 18 (): 18-26
3 20301353 2021 Yu-Wai-Man, P., Chinnery, P. F. (2021) Leber hereditary optic neuropathy [updated 2021 Mar 11] GeneReviews® M. P. Adam, H. H. Ardinger, R. A. Pagon, S. E. Wallace, L. J. H. Bean, G. Mirza, A. Amemiya (): https://www.ncbi.nlm.nih.gov/books/NBK1174/ .
4 29253894 2017 Wei, W., Gomez-Duran, A., Hudson, G., Chinnery, P. F. (2017) Background sequence characteristics influence the occurrence and severity of disease-causing mtDNA mutations PLoS Genetics . 13 (12): e1007126 .
5 15972314 2006 Mitchell, A. L., Elson, J. L., Howell, N., Taylor, R. W., Turnbull, D. M. (2006) Sequence variation in mitochondrial complex I genes: mutation or polymorphism? Journal of Medical Genetics . 43 (2): 175-179 .
6 19497304 2009 Yang, J., Zhu, Y., Tong, Y., Chen, L., Liu, L., Zhang, Z., Wang, X., Huang, D., Qiu, W., Zhuang, S., Ma, X. (2009) Confirmation of the mitochondrial ND1 gene mutation G3635A as a primary LHON mutation Biochemical and Biophysical Research Communications . 386 (1): 50-54 .
7 21074518 2010 Jia, X., Li, S., Wang, P., Guo, X., Zhang, Q. (2010) mtDNA m.3635G>A may be classified as a common primary mutation for Leber hereditary optic neuropathy in the Chinese population Biochemical and Biophysical Research Communications . 403 (2): 237-241 .
8 19527690 2009 Zhang, A. M., Zou, Y., Guo, X., Jia, X., Zhang, Q., Yao, Y. G. (2009) Mitochondrial DNA mutation m.3635G>A may be associated with Leber hereditary optic neuropathy in Chinese Biochemical and Biophysical Research Communications . 386 (2): 392-395 .
9 NA 2009 Shi, X. L., Hu, Z. M., Du, L. P., Jin, X. M., Xia, K. (2009) The coexistence of a novel ND5 A12340G mutation with ND1 G3635A mutation in a Chinese family with Leber hereditary optic neuropathy Academic Conference of Chinese Medical Association, Ophthalmology Department Branch . Online publication (http://www.medcon.org.cn/2009/cmao/cn/news.asp?abid=3238.html): . .
10 23304069 2012 Bi, R., Zhang, A. M., Jia, X., Zhang, Q., Yao, Y. G. (2012) Complete mitochondrial DNA genome sequence variation of Chinese families with mutation m.3635G>A and Leber hereditary optic neuropathy Molecular Vision . 18 (): 3087-3094 .
11 27177320 2016 Ji, Y., Liang, M., Zhang, J., Zhu, L., Zhang, Z., Fu, R., Liu, X., Zhang, M., Fu, Q., Zhao, F., Tong, Y., Sun, Y., Jiang, P., Guan, M. X. (2016) Mitochondrial ND1 Variants in 1281 Chinese Subjects With Leber's hereditary optic neuropathy Investigative Ophthalmology and Visual Science . 57 (6): 2377-2789 .
12 29387390 2018 Dai, Y., Wang, C., Nie, Z., Han, J., Chen, T., Zhao, X., Ai, C., Ji, Y., Gao, T., Jiang, P. (2018) Mutation analysis of Leber's hereditary optic neuropathy using a multi-gene panel Biomedical Reports . 8 (1): 51-58 .
13 31817256 2019 Starikovskaya, E., Shalaurova, S., Dryomov, S., Nazhmidenova, A., Volodko, N., Bychkov, I., Mazunin, I., Sukernik, R. (2019) Mitochondrial DNA Variation of Leber's hereditary optic neuropathy in Western Siberia Cells . 8 (12): e1574 .
14 32652755 2020 Wong, L. C., Chen, T., Schmitt, E. S., Wang, J., Tang, S., Landsverk, M., Li, F., Zhang, S., Wang, Y., Zhang, V. W., Craigen, W. J. (2020) Clinical and laboratory interpretation of mitochondrial mRNA variants Human Mutatation . 41 (10): .
15 33417421 2021 Birnbaum, F. A., Gospe, S. M., 3rd (2021) Severe Leber hereditary optic neuropathy plus disease in a middle-aged man Journal of Neuro-Ophthalmology . ePub ahead of print, http://doi.org/10.1097/WNO.0000000000001151 (): .
16 NA 2022 Lackey, E., Lefland, A., Eckstein, C. (2022) Leber's hereditary optic neuropathy plus causing recurrent myelopathy due to an MT-DN1 mutation at G3635A Case Reports in Neurological Medicine 2022 (): https://doi.org/10.1155/2022/1628892 .