APA (7th ed.) Citation

Y, P., DN, S., CA, V., JS, M., J, R., M, T. C., . . . T, H. (2017). Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy. Human molecular genetics, 26(24), 4937. https://doi.org/10.1093/hmg/ddx377

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 26, no. 24 (2017): 4937. https://doi.org/10.1093/hmg/ddx377.

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. 26, no. 24, 2017, p. 4937, https://doi.org/10.1093/hmg/ddx377.