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Dive into the research topics of 'Lattice corneal dystrophy type 1 in a Canadian kindred is associated with the Arg124 → Cys mutation in the kerato-epithelin gene'. Together they form a unique fingerprint.- Sort by
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Sanjoy K. Gupta, William G. Hodge, Karim F. Damji, Duane L. Guernsey, Paul E. Neumann
Research output: Contribution to journal › Article › peer-review