Adachi, R., Shoji, J., Yuda, K., Shimizu, T., Hara, Y., Tomioka, A., . . . Yamagami, S. (2025). Unilateral lattice corneal dystrophy with c.1501C>A (p.P501T) and c.1733T>C (p.L578P) variants in the transforming growth factor-beta induced gene: A case report. Ophthalmic Genetics, 46(1), 83. https://doi.org/10.1080/13816810.2024.2434038
Chicago Style (17th ed.) CitationAdachi, Rumi, Jun Shoji, Kentaro Yuda, Toshiki Shimizu, Yusuke Hara, Akiko Tomioka, Noriko Inada, Takahiko Hayashi, and Satoru Yamagami. "Unilateral Lattice Corneal Dystrophy with C.1501C>A (p.P501T) and C.1733T>C (p.L578P) Variants in the Transforming Growth Factor-beta Induced Gene: A Case Report." Ophthalmic Genetics 46, no. 1 (2025): 83. https://doi.org/10.1080/13816810.2024.2434038.
MLA (9th ed.) CitationAdachi, Rumi, et al. "Unilateral Lattice Corneal Dystrophy with C.1501C>A (p.P501T) and C.1733T>C (p.L578P) Variants in the Transforming Growth Factor-beta Induced Gene: A Case Report." Ophthalmic Genetics, vol. 46, no. 1, 2025, p. 83, https://doi.org/10.1080/13816810.2024.2434038.