Lattice corneal dystrophy type 1 in a Canadian kindred is associated with the Arg124 → Cys mutation in the kerato-epithelin gene

Authors

Sanjoy K. Gupta, Dalhousie University, United States
William G. Hodge, University of Ottawa Eye Institute, Canada
Karim F. Damji, University of Ottawa Eye Institute, CanadaFollow
Duane L. Guernsey, Dalhousie University, United States
Paul E. Neumann, Dalhousie University, United States

Document Type

Report

Department

Ophthalmology

Comments

This work was published before the author joined Aga Khan University.

Publication (Name of Journal)

American Journal of Ophthalmology

Recommended Citation

Gupta, S. K., Hodge, W. G., Damji, K. F., Guernsey, D. L., Neumann, P. E. (1998). Lattice corneal dystrophy type 1 in a Canadian kindred is associated with the Arg124 → Cys mutation in the kerato-epithelin gene. American Journal of Ophthalmology, 125(4), 547-549.
Available at: https://ecommons.aku.edu/pakistan_fhs_mc_ophthalmol/134