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Lattice corneal dystrophy, gelsolin type (Meretoja’s syndrome)

✍ Scribed by Christian Carrwik; Ulf Stenevi

Book ID: 118075834
Publisher: Wiley (Blackwell Publishing)
Year: 2009
Tongue: English
Weight: 254 KB
Volume: 87
Category: Article
ISSN: 1755-375X
DOI: 10.1111/j.1755-3768.2009.01686.x

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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