A new mutation (A546T) of the βig-h3 gene responsible for a French lattice corneal dystrophy type IIIA
- 29 February 2000
- journal article
- research article
- Published by Elsevier in American Journal of Ophthalmology
- Vol. 129 (2) , 248-251
- https://doi.org/10.1016/s0002-9394(99)00324-4
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- A Kerato-Epithelin (βig-h3) Mutation in Lattice Corneal Dystrophy Type IIIAAmerican Journal of Human Genetics, 1998
- Mutation Hot Spots in 5q31-Linked Corneal DystrophiesAmerican Journal of Human Genetics, 1998
- Kerato-epithelin mutations in four 5q31-linked corneal dystrophiesNature Genetics, 1997
- Lattice Corneal Dystrophy Type IIIAArchives of Ophthalmology (1950), 1991