Advances in the molecular genetics of corneal dystrophies

This publication has 47 references indexed in Scilit:

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• The classic form of granular corneal dystrophy associated with R555W mutation in the BIGH3 gene is rare in Japanese patients
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• Lattice corneal dystrophy type 1 in a Canadian kindred is associated with the Arg124 → Cys mutation in the kerato-epithelin gene
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• Homogeneity of Kerato-Epithelin Codon 124 Mutations in Japanese Patients with Either of Two Types of Corneal Stromal Dystrophy
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• Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy
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• Kerato-epithelin mutations in four 5q31-linked corneal dystrophies
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