APA (7th ed.) Citation

A, C., R, H., AZ, M., M, G., HM, L., K, U., . . . H, O. (2019). Mutations in MAP3K1 that cause 46,XY disorders of sex development disrupt distinct structural domains in the protein. Human molecular genetics, 28(10), 1620. https://doi.org/10.1093/hmg/ddz002

Chicago Style (17th ed.) Citation

A, Chamberlin, et al. "Mutations in MAP3K1 That Cause 46,XY Disorders of Sex Development Disrupt Distinct Structural Domains in the Protein." Human Molecular Genetics 28, no. 10 (2019): 1620. https://doi.org/10.1093/hmg/ddz002.

MLA (9th ed.) Citation

A, Chamberlin, et al. "Mutations in MAP3K1 That Cause 46,XY Disorders of Sex Development Disrupt Distinct Structural Domains in the Protein." Human Molecular Genetics, vol. 28, no. 10, 2019, p. 1620, https://doi.org/10.1093/hmg/ddz002.