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

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Eranga N. Vithana

Singapore Eye Research Institute

11 Third Hospital Avenue

Singapore 168751

Singapore

[email]@yahoo.co.uk

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Affiliation

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

References

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]
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]