S.K. Gupta
Department of Pathology
Dalhousie University
Ottawa
Ontario
Canada
Name/email consistency: high
- A novel PAX6 frameshift mutation in a kindred from Atlantic Canada with familial aniridia. Gupta, S.K., Orr, A., Bulman, D., De Becker, I., Guernsey, D.L., Neumann, P.E. Can. J. Ophthalmol. (1999)
- Lattice corneal dystrophy type 1 in a Canadian kindred is associated with the Arg124 --> Cys mutation in the kerato-epithelin gene. sgupta@ogh.on.ca. Gupta, S.K., Hodge, W.G., Damji, K.F., Guernsey, D.L., Neumann, P.E. Am. J. Ophthalmol. (1998)