Browsing by Author Casey, J.R.

Showing results 1 to 6 of 6
Issue DateTitleAuthor(s)
2007Identification and characterization of a novel mutation in the carbonic anhydrase IV gene that causes retinitis pigmentosaAlvarez, B.V.; Casey, J.R.; Shandro, H.J.; Vithana, E.N. ; Yeung, K.; Yong, V.; Aung, T. ; Yang, Z.; Chen, Y.; Zhang, K.; Koh, A.H.; Kolatkar, P.; Palasingam, P.
Aug-2007Identification and characterization of a novel mutation in the carbonic anhydrase IV gene that causes retinitis pigmentosaAlvarez, B.V.; Vithana, E.N. ; Yang, Z.; Koh, A.H.; Yeung, K.; Yong, V.; Shandro, H.J.; Chen, Y.; Kolatkar, P. ; Palasingam, P.; Zhang, K.; Aung, T. ; Casey, J.R.
2006Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)Vithana, E.N. ; Tan, D.T.H. ; Yong, V.H.K.; Morgan, P.; Casey, J.R.; Sundaresan, P.; Hemadevi, B.; Srinivasan, M.; Prajna, V.; Ebenezer, N.D.; Mohamed, M.D.; Inglehearn, C.F.; Anand, S.; Khine, K.O.; Khine, M.; Salto-Tellez, M. ; Guo, K.
2006Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)Vithana, E.N. ; Tan, D.T.H. ; Venkataraman, D.; Yong, V.H.K.; Aung, T. ; Morgan, P.; Casey, J.R.; Sundaresan, P.; Hemadevi, B.; Srinivasan, M.; Prajna, V.; Ebenezer, N.D.; Mohamed, M.D.; Inglehearn, C.F.; Anand, S.; Khine, K.O.; Salto-Tellez, M. ; Guo, K.
2008SLC4A11 mutations in Fuchs endothelial corneal dystrophyVithana, E.N. ; Tan, D.T.H. ; Venkataraman, D.; Venkatraman, A.; Aung, T. ; Morgan, P.E.; Casey, J.R.; Ramprasad, V.; Nagasamy, S.; Kumaramanickevel, G.; Rajagopal, R.; Yam, G.H.F.; Law, R.W.K.; Pang, C.P.; Yong, V.H.K
Nov-2013Transmembrane water-flux through SLC4A11: A route defective in genetic corneal diseasesVilas, G.L.; Loganathan, S.K.; Liu, J.; Riau, A.K.; Young, J.D.; Mehta, J.S. ; Vithana, E.N.; Casey, J.R.