Peng, Y., Shinde, D. N., Valencia, C. A., Mo, J., Rosenfeld, J., Truitt Cho, M., Chamberlin, A., Li, Z., Liu, J., Gui, B., Brockhage, R., Basinger, A., Alvarez-Leon, B., Heydemann, P., Magoulas, P. L., Lewis, A. M., Scaglia, F., Gril, S., Chong, S. C., Bower, M., Monaghan, K. G., Willaert, R., Plona, M., Dineen, R., Milan, F., Hoganson, G., Powis, Z., Helbig, K. L., Keller-Ramey, J., Harris, B., Anderson, L. C., Green, T., Sukoff Rizzo, S. J., Kaylor, J., Chen, J., Guan, M., Sellars, E., Sparagana, S. P., Gibson, J. B., Reinholdt, L. G., Tang, S., & Huang, T. (n.d.). biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy. Human molecular genetics, 26, 4937–4950. http://access.bl.uk/ark:/81055/vdc_100173696418.0x000026