Homogeneity of Kerato-Epithelin Codon 124 Mutations in Japanese Patients with Either of Two Types of Corneal Stromal Dystrophy
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics
Reference19 articles.
1. Granular dystrophy of the cornea: characteristic electron microscopic lesion;Akiya;Arch Ophthalmol,1970
2. Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations;Brown;Hum Mutat,1995
3. Clinically atypical granular corneal dystrophy with pathological features of lattice-like amyloid deposits: a study of three families;Folberg;Ophthalmology,1988
4. The relationship between granular, lattice type 1, and Avellino corneal dystrophies: a histopathologic study;Folberg;Arch Ophthalmol,1994
5. A homozygous 1–base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese;Fuchs;Nat Genet,1995
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