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

Please use this identifier to cite or link to this item: https://doi.org/10.1038/ng1824

Title:	Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)
Authors:	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
Issue Date:	2006
Citation:	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 (2006). Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2). Nature Genetics 38 (7) : 755-757. ScholarBank@NUS Repository. https://doi.org/10.1038/ng1824
Source Title:	Nature Genetics
URI:	http://scholarbank.nus.edu.sg/handle/10635/33171
ISSN:	10614036 15461718
DOI:	10.1038/ng1824
Appears in Collections:	Staff Publications

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