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A case of lattice corneal dystrophy due to L527R mutation in theTGFBIgene with asymmetric corneal opacity in eye laterality

✍ Scribed by Takako Ohnishi; Tohru Sakimoto; Mitsuru Sawa

Book ID: 106327814
Publisher: Springer
Year: 2010
Tongue: English
Weight: 159 KB
Volume: 54
Category: Article
ISSN: 0021-5155
DOI: 10.1007/s10384-010-0882-1

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