Lattice corneal dystrophy type 1 in a Canadian kindred is associated with the Arg124 → Cys mutation in the kerato-epithelin gene
Document Type
Report
Department
Ophthalmology
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
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Comments
This work was published before the author joined Aga Khan University.