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.
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| Title: | 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. |
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| Authors: | Adachi, Rumi1 (AUTHOR), Shoji, Jun1,2 (AUTHOR), Yuda, Kentaro3 (AUTHOR), Shimizu, Toshiki1 (AUTHOR), Hara, Yusuke1 (AUTHOR), Tomioka, Akiko1 (AUTHOR), Inada, Noriko1 (AUTHOR), Hayashi, Takahiko1 (AUTHOR), Yamagami, Satoru1 (AUTHOR) yamagami.satoru@nihon-u.ac.jp |
| Source: | Ophthalmic Genetics. Feb2025, Vol. 46 Issue 1, p83-88. 6p. |
| Database: | Academic Search Ultimate |
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