W, v. L., S, S., J, W., R, H., A, C., D, S., . . . FP, R. (2023). Systematically testing human HMBS missense variants to reveal mechanism and pathogenic variation. American journal of human genetics, 110(10), 1769. https://doi.org/10.1016/j.ajhg.2023.08.012
Chicago Style (17th ed.) CitationW, van Loggerenberg, et al. "Systematically Testing Human HMBS Missense Variants to Reveal Mechanism and Pathogenic Variation." American Journal of Human Genetics 110, no. 10 (2023): 1769. https://doi.org/10.1016/j.ajhg.2023.08.012.
MLA (9th ed.) CitationW, van Loggerenberg, et al. "Systematically Testing Human HMBS Missense Variants to Reveal Mechanism and Pathogenic Variation." American Journal of Human Genetics, vol. 110, no. 10, 2023, p. 1769, https://doi.org/10.1016/j.ajhg.2023.08.012.