Lattice corneal dystrophy type 1 in a Canadian kindred is associated with the Arg124 → Cys mutation in the kerato-epithelin gene
- 1 April 1998
- journal article
- case report
- Published by Elsevier in American Journal of Ophthalmology
- Vol. 125 (4) , 547-549
- https://doi.org/10.1016/s0002-9394(99)80196-2
Abstract
No abstract availableKeywords
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- Mapping of Reis-Bücklers' Corneal Dystrophy to Chromosome 5qAmerican Journal of Ophthalmology, 1996
- Three autosomal dominant corneal dystrophies map to chromosome 5qNature Genetics, 1994
- Genetic aspects of familial amyloidosis with corneal lattice dystrophy and cranial neuropathyClinical Genetics, 1973
- The Lattice Type of Familial Corneal DegenerationA.M.A. Archives of Ophthalmology, 1959