APA (7th ed.) Citation

SP, L., C, S., M, H., A, B., E, M., I, M., . . . R, H. (2026). Incomplete congenital stationary night blindness associated with a novel variant in the CACNA1F gene. Documenta ophthalmologica. Advances in ophthalmology, 152(3), 401. https://doi.org/10.1007/s10633-025-10062-x

Chicago Style (17th ed.) Citation

SP, Loo, Shipton C, Hamilton M, Brown A, Millar E, Malik I, Craig M, and Hamilton R. "Incomplete Congenital Stationary Night Blindness Associated with a Novel Variant in the CACNA1F Gene." Documenta Ophthalmologica. Advances in Ophthalmology 152, no. 3 (2026): 401. https://doi.org/10.1007/s10633-025-10062-x.

MLA (9th ed.) Citation

SP, Loo, et al. "Incomplete Congenital Stationary Night Blindness Associated with a Novel Variant in the CACNA1F Gene." Documenta Ophthalmologica. Advances in Ophthalmology, vol. 152, no. 3, 2026, p. 401, https://doi.org/10.1007/s10633-025-10062-x.