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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Eranga N. Vithana

Singapore Eye Research Institute

11 Third Hospital Avenue

Singapore 168751



Name/email consistency: high



  • Singapore Eye Research Institute, 11 Third Hospital Avenue, Singapore 168751, Singapore. 2006 - 2008


  1. SLC4A11 mutations in Fuchs endothelial corneal dystrophy. Vithana, E.N., Morgan, P.E., Ramprasad, V., Tan, D.T., Yong, V.H., Venkataraman, D., Venkatraman, A., Yam, G.H., Nagasamy, S., Law, R.W., Rajagopal, R., Pang, C.P., Kumaramanickevel, G., Casey, J.R., Aung, T. Hum. Mol. Genet. (2008) [Pubmed]
  2. Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2). Vithana, E.N., Morgan, P., Sundaresan, P., Ebenezer, N.D., Tan, D.T., Mohamed, M.D., Anand, S., Khine, K.O., Venkataraman, D., Yong, V.H., Salto-Tellez, M., Venkatraman, A., Guo, K., Hemadevi, B., Srinivasan, M., Prajna, V., Khine, M., Casey, J.R., Inglehearn, C.F., Aung, T. Nat. Genet. (2006) [Pubmed]
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