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Lattice Corneal Dystrophy Type III in Patients with a Homozygous L527R Mutation in theTGFBIGene

✍ Scribed by Tomoyo Funayama; Yukihiko Mashima; Motoko Kawashima; Masakazu Yamada


Book ID
118297867
Publisher
Springer
Year
2006
Tongue
English
Weight
197 KB
Volume
50
Category
Article
ISSN
0021-5155

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## Abstract Lattice corneal dystrophies (LCDs) are caused by mutations of the transforming growth factor beta‐induced gene (__TGFBI__, formerly __Ξ²ig‐h3__). LCD type IIIA (LCDIIIA) has been reported mostly from Japan. In this study, we demonstrate allelic homogeneity for Japanese patients with LCDI