MITOMAP References for Mutation T-C at 8639

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1 23463613 2013 Tang, S., Wang, J., Zhang, W., Li, F., Landsverk, M., Cui, H., Truong, C., Wang, G., Li, C., Graham, B., Scaglia, F., Schmitt, E. S., Craigen, W. J., Wong, L. C. (2013) Transition to next generation analysis of the whole mitochondrial genome: a summary of molecular defects Human Mutation . 34 (6): 882-893 Most reported SNVs are not found in the body of the paper itself but are listed in the supplemental information as Unclassified Variants.
2 31743754 2020 Jancic, J., Rovcanin, B., Djuric, V., Pepic, A., Samardzic, J., Nikolic, B., Novakovic, I., Kostic, V. S. (2020) Analysis of secondary mtDNA mutations in families with Leber's hereditary optic neuropathy: Four novel variants and their association with clinical presentation Mitochondrion . 50 (): 132-138 .