APA (7th ed.) Citation

K, B., J, S., S, L., J, C., D, D. S., A, K., . . . A, B. (2016). The molecular basis of variable phenotypic severity among common missense mutations causing Rett syndrome. Human molecular genetics, 25(3), 558. https://doi.org/10.1093/hmg/ddv496

Chicago Style (17th ed.) Citation

K, Brown, et al. "The Molecular Basis of Variable Phenotypic Severity Among Common Missense Mutations Causing Rett Syndrome." Human Molecular Genetics 25, no. 3 (2016): 558. https://doi.org/10.1093/hmg/ddv496.

MLA (9th ed.) Citation

K, Brown, et al. "The Molecular Basis of Variable Phenotypic Severity Among Common Missense Mutations Causing Rett Syndrome." Human Molecular Genetics, vol. 25, no. 3, 2016, p. 558, https://doi.org/10.1093/hmg/ddv496.