APA (7th ed.) Citation

Yang-Seeger, D., Pauleikhoff, L. J. B., Atiskova, Y., Thiele, S., Spitzer, M. S., & Birtel, J. (2025). C1QTNF5 missense variant causing autosomal dominant gyrate atrophy-like choroidal dystrophy. Ophthalmic Genetics, 46(4), 397. https://doi.org/10.1080/13816810.2025.2492037

Chicago Style (17th ed.) Citation

Yang-Seeger, Denise, Laurenz J. B. Pauleikhoff, Yevgeniya Atiskova, Sarah Thiele, Martin S. Spitzer, and Johannes Birtel. "C1QTNF5 Missense Variant Causing Autosomal Dominant Gyrate Atrophy-like Choroidal Dystrophy." Ophthalmic Genetics 46, no. 4 (2025): 397. https://doi.org/10.1080/13816810.2025.2492037.

MLA (9th ed.) Citation

Yang-Seeger, Denise, et al. "C1QTNF5 Missense Variant Causing Autosomal Dominant Gyrate Atrophy-like Choroidal Dystrophy." Ophthalmic Genetics, vol. 46, no. 4, 2025, p. 397, https://doi.org/10.1080/13816810.2025.2492037.