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.
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

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spelling	sg-nus-scholar.10635-331712023-10-26T20:37:04Z 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. 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. (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.
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.
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. 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_	1781410831992356864

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

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