APA (7th ed.) Citation

Morgan, N. V., Hartley, J. L., Setchell, K. D. R., Simpson, M. A., Brown, R., Tee, L., . . . Kelly, D. A. (2013). A combination of mutations in AKR1D1 and SKIV2L in a family with severe infantile liver disease. Orphanet Journal of Rare Diseases, 8(1), 1. https://doi.org/10.1186/1750-1172-8-74

Chicago Style (17th ed.) Citation

Morgan, Neil V., et al. "A Combination of Mutations in AKR1D1 and SKIV2L in a Family with Severe Infantile Liver Disease." Orphanet Journal of Rare Diseases 8, no. 1 (2013): 1. https://doi.org/10.1186/1750-1172-8-74.

MLA (9th ed.) Citation

Morgan, Neil V., et al. "A Combination of Mutations in AKR1D1 and SKIV2L in a Family with Severe Infantile Liver Disease." Orphanet Journal of Rare Diseases, vol. 8, no. 1, 2013, p. 1, https://doi.org/10.1186/1750-1172-8-74.