The classic form of granular corneal dystrophy associated with R555W mutation in the BIGH3 gene is rare in Japanese patients
- 1 September 1998
- journal article
- case report
- Published by Elsevier in American Journal of Ophthalmology
- Vol. 126 (3) , 450-452
- https://doi.org/10.1016/s0002-9394(98)00105-6
Abstract
No abstract availableKeywords
This publication has 3 references indexed in Scilit:
- Homogeneity of Kerato-Epithelin Codon 124 Mutations in Japanese Patients with Either of Two Types of Corneal Stromal DystrophyAmerican Journal of Human Genetics, 1997
- Kerato-epithelin mutations in four 5q31-linked corneal dystrophiesNature Genetics, 1997
- Inter‐familial variability and intra‐familial similarities of granular corneal dystrophy Groenouw type I with respect to biomicroscopical appearance and symptomatologyActa Ophthalmologica, 1989