Association of autosomal dominantly inherited corneal dystrophies with BIGH3 gene mutations in Japan
Author:
Publisher
Elsevier BV
Subject
Ophthalmology
Reference5 articles.
1. Kerato-epithelin mutations in four 5q31-linked corneal dystrophies;Munier;Nat Genet,1997
2. A kerato-epithelin (betaig-h3) mutation in lattice corneal dystrophy type IIIA;Yamamoto;Am J Hum Genet,1998
3. A new L527R mutation of the betaIGH3 gene in patients with lattice corneal dystrophy with deep stromal opacities;Fujiki;Hum Genet,1998
4. Reevaluation of corneal dystrophies of Bowman’s layer and the anterior stroma (Reis-Bücklers and Thiel–Behnke Type);Küchle;Cornea,1995
5. A novel mutation at the Codon 124 in the BIGH3 gene is associated with a superficial granular corneal dystrophy;Mashima;Arch Ophthalmol,1999
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