Please use this identifier to cite or link to this item: https://doi.org/10.1093/hmg/ddm337
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dc.titleSLC4A11 mutations in Fuchs endothelial corneal dystrophy
dc.contributor.authorVithana, E.N.
dc.contributor.authorTan, D.T.H.
dc.contributor.authorVenkataraman, D.
dc.contributor.authorVenkatraman, A.
dc.contributor.authorAung, T.
dc.contributor.authorMorgan, P.E.
dc.contributor.authorCasey, J.R.
dc.contributor.authorRamprasad, V.
dc.contributor.authorNagasamy, S.
dc.contributor.authorKumaramanickevel, G.
dc.contributor.authorRajagopal, R.
dc.contributor.authorYam, G.H.F.
dc.contributor.authorLaw, R.W.K.
dc.contributor.authorPang, C.P.
dc.contributor.authorYong, V.H.K
dc.date.accessioned2011-09-26T09:05:15Z
dc.date.available2011-09-26T09:05:15Z
dc.date.issued2008
dc.identifier.citationVithana, E.N., Tan, D.T.H., Venkataraman, D., Venkatraman, A., Aung, T., Morgan, P.E., Casey, J.R., Ramprasad, V., Nagasamy, S., Kumaramanickevel, G., Rajagopal, R., Yam, G.H.F., Law, R.W.K., Pang, C.P., Yong, V.H.K (2008). SLC4A11 mutations in Fuchs endothelial corneal dystrophy. Human Molecular Genetics 17 (5) : 656-666. ScholarBank@NUS Repository. https://doi.org/10.1093/hmg/ddm337
dc.identifier.issn09646906
dc.identifier.issn14602083
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/26493
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentOPHTHALMOLOGY
dc.description.doi10.1093/hmg/ddm337
dc.description.sourcetitleHuman Molecular Genetics
dc.description.volume17
dc.description.issue5
dc.description.page656-666
dc.identifier.isiut000253490600003
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