APA (7th ed.) Citation

Y, P., DN, S., C, A. V., JS, M., J, R., MT, C., . . . B, G. (2018). Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy. Human molecular genetics, 27(12), 2224. https://doi.org/10.1093/hmg/ddy072

Chicago Style (17th ed.) Citation

Y, Peng, et al. "Biallelic Mutations in the Ferredoxin Reductase Gene Cause Novel Mitochondriopathy with Optic Atrophy." Human Molecular Genetics 27, no. 12 (2018): 2224. https://doi.org/10.1093/hmg/ddy072.

MLA (9th ed.) Citation

Y, Peng, et al. "Biallelic Mutations in the Ferredoxin Reductase Gene Cause Novel Mitochondriopathy with Optic Atrophy." Human Molecular Genetics, vol. 27, no. 12, 2018, p. 2224, https://doi.org/10.1093/hmg/ddy072.