Please use this identifier to cite or link to this item: https://doi.org/10.1038/ng1824
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dc.titleMutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)
dc.contributor.authorVithana, E.N.
dc.contributor.authorTan, D.T.H.
dc.contributor.authorYong, V.H.K.
dc.contributor.authorMorgan, P.
dc.contributor.authorCasey, J.R.
dc.contributor.authorSundaresan, P.
dc.contributor.authorHemadevi, B.
dc.contributor.authorSrinivasan, M.
dc.contributor.authorPrajna, V.
dc.contributor.authorEbenezer, N.D.
dc.contributor.authorMohamed, M.D.
dc.contributor.authorInglehearn, C.F.
dc.contributor.authorAnand, S.
dc.contributor.authorKhine, K.O.
dc.contributor.authorKhine, M.
dc.contributor.authorSalto-Tellez, M.
dc.contributor.authorGuo, K.
dc.date.accessioned2012-05-29T02:21:31Z
dc.date.available2012-05-29T02:21:31Z
dc.date.issued2006
dc.identifier.citationVithana, 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
dc.identifier.issn10614036
dc.identifier.issn15461718
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/33171
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1038/ng1824
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentOPHTHALMOLOGY
dc.contributor.departmentPATHOLOGY
dc.description.doi10.1038/ng1824
dc.description.sourcetitleNature Genetics
dc.description.volume38
dc.description.issue7
dc.description.page755-757
dc.description.codenNGENE
dc.identifier.isiut000238669300010
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