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. - Adachi, Rumi; Shoji, Jun; Yuda, Kentaro; Shimizu, Toshiki; Hara, Yusuke; Tomioka, Akiko; Inada, Noriko; Hayashi, Takahiko; Yamagami, Satoru (Ophthalmic Genetics, 2025)