Transmembrane water-flux through SLC4A11: A route defective in genetic corneal diseases

by Vilas, G.L., Loganathan, S.K., Liu, J., Riau, A.K., Young, J.D., Mehta, J.S., Vithana, E.N., Casey, J.R.
Published 2014

Identification and characterization of a novel mutation in the carbonic anhydrase IV gene that causes retinitis pigmentosa

by Alvarez, 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.
Published 2016

SLC4A11 mutations in Fuchs endothelial corneal dystrophy

by Vithana, 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
Published 2011

Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)

by 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., Aung Tin
Published 2012