Cite
Clinical and genetic findings in TRPM1‐related congenital stationary night blindness.
MLA
Iosifidis, Christos, et al. “Clinical and Genetic Findings in TRPM1‐related Congenital Stationary Night Blindness.” Acta Ophthalmologica (1755375X), vol. 100, no. 6, Sept. 2022, pp. e1332–39. EBSCOhost, https://doi.org/10.1111/aos.15186.
APA
Iosifidis, C., Liu, J., Gale, T., Ellingford, J. M., Campbell, C., Ingram, S., Chandler, K., Parry, N. R. A., Black, G. C., & Sergouniotis, P. I. (2022). Clinical and genetic findings in TRPM1‐related congenital stationary night blindness. Acta Ophthalmologica (1755375X), 100(6), e1332–e1339. https://doi.org/10.1111/aos.15186
Chicago
Iosifidis, Christos, Jingshu Liu, Theodora Gale, Jamie M. Ellingford, Christopher Campbell, Stuart Ingram, Kate Chandler, Neil R. A. Parry, Graeme C. Black, and Panagiotis I. Sergouniotis. 2022. “Clinical and Genetic Findings in TRPM1‐related Congenital Stationary Night Blindness.” Acta Ophthalmologica (1755375X) 100 (6): e1332–39. doi:10.1111/aos.15186.