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

10.1038/ng1824

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Main 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
Other Authors:	OPHTHALMOLOGY
Format:	Article
Published:	2012
Online Access:	http://scholarbank.nus.edu.sg/handle/10635/33171
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Institution:	National University of Singapore

id	sg-nus-scholar.10635-33171
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spelling	sg-nus-scholar.10635-331712024-11-15T16:22:43Z Mutations 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. Aung Tin OPHTHALMOLOGY PATHOLOGY 10.1038/ng1824 Nature Genetics 38 7 755-757 NGENE 2012-05-29T02:21:31Z 2012-05-29T02:21:31Z 2006 Article 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 10614036 15461718 http://scholarbank.nus.edu.sg/handle/10635/33171 000238669300010 Scopus
institution	National University of Singapore
building	NUS Library
continent	Asia
country	Singapore Singapore
content_provider	NUS Library
collection	ScholarBank@NUS
description	10.1038/ng1824
author2	OPHTHALMOLOGY
author_facet	OPHTHALMOLOGY 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
format	Article
author	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
spellingShingle	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 Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)
author_sort	Vithana, E.N.
title	Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)
title_short	Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)
title_full	Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)
title_fullStr	Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)
title_full_unstemmed	Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)
title_sort	mutations in sodium-borate cotransporter slc4a11 cause recessive congenital hereditary endothelial dystrophy (ched2)
publishDate	2012
url	http://scholarbank.nus.edu.sg/handle/10635/33171
_version_	1821219512777703424

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

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