APA (7th ed.) Citation

NS, L., CL, F., Z, S., & K, A. (2026). Novel heterozygous UCHL1 variant causing severe optic atrophy and vision loss. Ophthalmic genetics, 1. https://doi.org/10.1080/13816810.2026.2655887

Chicago Style (17th ed.) Citation

NS, Lee, Fraser CL, Stark Z, and Ahmad K. "Novel Heterozygous UCHL1 Variant Causing Severe Optic Atrophy and Vision Loss." Ophthalmic Genetics 2026: 1. https://doi.org/10.1080/13816810.2026.2655887.

MLA (9th ed.) Citation

NS, Lee, et al. "Novel Heterozygous UCHL1 Variant Causing Severe Optic Atrophy and Vision Loss." Ophthalmic Genetics, 2026, p. 1, https://doi.org/10.1080/13816810.2026.2655887.