Cite
A recurrent synonymous mutation in the human androgen receptor gene causing complete androgen insensitivity syndrome.
MLA
Batista, Rafael Loch, et al. “A Recurrent Synonymous Mutation in the Human Androgen Receptor Gene Causing Complete Androgen Insensitivity Syndrome.” The Journal of Steroid Biochemistry and Molecular Biology, vol. 174, Nov. 2017, pp. 14–16. EBSCOhost, https://doi.org/10.1016/j.jsbmb.2017.07.020.
APA
Batista, R. L., Rodrigues, A. di S., Nishi, M. Y., Gomes, N. L., Faria, J. A. D. J., Moraes, D. R. de, Carvalho, L. R., Costa, E. M. F., Domenice, S., & Mendonca, B. B. (2017). A recurrent synonymous mutation in the human androgen receptor gene causing complete androgen insensitivity syndrome. The Journal of Steroid Biochemistry and Molecular Biology, 174, 14–16. https://doi.org/10.1016/j.jsbmb.2017.07.020
Chicago
Batista, Rafael Loch, Andresa di Santi Rodrigues, Mirian Yumie Nishi, Nathalia Lisboa Gomes, José Antonio Diniz, Junior Faria, Daniela Rodrigues de Moraes, Luciani Renata Carvalho, Elaine Maria Frade Costa, Sorahia Domenice, and Berenice Bilharinho Mendonca. 2017. “A Recurrent Synonymous Mutation in the Human Androgen Receptor Gene Causing Complete Androgen Insensitivity Syndrome.” The Journal of Steroid Biochemistry and Molecular Biology 174 (November): 14–16. doi:10.1016/j.jsbmb.2017.07.020.