A Kerato-Epithelin (βig-h3) Mutation in Lattice Corneal Dystrophy Type IIIA
- 1 March 1998
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 62 (3) , 719-722
- https://doi.org/10.1086/301765
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Kerato-epithelin mutations in four 5q31-linked corneal dystrophiesNature Genetics, 1997
- βig-h3: A Transforming Growth Factor-β-Responsive Gene Encoding a Secreted Protein That Inhibits Cell AttachmentIn Vitroand Suppresses the Growth of CHO Cells in Nude MiceDNA and Cell Biology, 1994
- Three autosomal dominant corneal dystrophies map to chromosome 5qNature Genetics, 1994
- cDNA Cloning and Sequence Analysis of βig-h3, a Novel Gene Induced in a Human Adenocarcinoma Cell Line after Treatment with Transforming Growth Factor-βDNA and Cell Biology, 1992
- Lattice Corneal Dystrophy Type IIIAArchives of Ophthalmology (1950), 1991
- Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms.Proceedings of the National Academy of Sciences, 1989
- Histopathologic and Immunochemical Features of Lattice Corneal Dystrophy Type IIIAmerican Journal of Ophthalmology, 1987
- Lack of Evidence for Protein Aa Reactivity in Amyloid Deposits of Lattice Corneal Dystrophy and Amyloid Corneal DegenerationAmerican Journal of Ophthalmology, 1984
- Comparative Histopathological and Clinical Findings in Eyes with Lattice Corneal Dystrophy of two Different TypesOphthalmologica, 1972