APA (7th ed.) Citation

SAW, S., FAN, Q., YOSHIMURA, N., KHOR, C., TAI, E., GOH, L., . . . LI, Y. (2011). CTNND2 is a genetic variant for high myopia. Acta Ophthalmologica (1755375X), 89, 0. https://doi.org/10.1111/j.1755-3768.2011.2222.x

Chicago Style (17th ed.) Citation

SAW, SM, Q. FAN, N. YOSHIMURA, CC KHOR, ES TAI, LK GOH, T. YOUNG, and YL LI. "CTNND2 Is a Genetic Variant for High Myopia." Acta Ophthalmologica (1755375X) 89 (2011). https://doi.org/10.1111/j.1755-3768.2011.2222.x.

MLA (9th ed.) Citation

SAW, SM, et al. "CTNND2 Is a Genetic Variant for High Myopia." Acta Ophthalmologica (1755375X), vol. 89, 2011, https://doi.org/10.1111/j.1755-3768.2011.2222.x.