APA (7th ed.) Citation

Coene, K. L., Roepman, R., Doherty, D., Afroze, B., Kroes, H. Y., Letteboer, S. J., . . . de Brouwer, A. P. (2009). OFD1 Is Mutated in X-Linked Joubert Syndrome and Interacts with LCA5-Encoded Lebercilin. American journal of human genetics, 85(4), 465-481. https://doi.org/10.1016/j.ajhg.2009.09.002

Chicago Style (17th ed.) Citation

Coene, Karlien L.M., et al. "OFD1 Is Mutated in X-Linked Joubert Syndrome and Interacts with LCA5-Encoded Lebercilin." American Journal of Human Genetics 85, no. 4 (2009): 465-481. https://doi.org/10.1016/j.ajhg.2009.09.002.

MLA (9th ed.) Citation

Coene, Karlien L.M., et al. "OFD1 Is Mutated in X-Linked Joubert Syndrome and Interacts with LCA5-Encoded Lebercilin." American Journal of Human Genetics, vol. 85, no. 4, 2009, pp. 465-481, https://doi.org/10.1016/j.ajhg.2009.09.002.