Please use this identifier to cite or link to this item: https://doi.org/10.1177/08830738060210021101
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dc.titleDiagnostic strategy for the detection of dystrophin gene mutations in Asian patients and carriers using immortalized cell lines
dc.contributor.authorTay, S.K.H.
dc.contributor.authorKhng, H.H.
dc.contributor.authorLow, P.S.
dc.contributor.authorLai, P.S.
dc.date.accessioned2011-08-16T07:42:59Z
dc.date.available2011-08-16T07:42:59Z
dc.date.issued2006
dc.identifier.citationTay, S.K.H.,Khng, H.H.,Low, P.S.,Lai, P.S. (2006). Diagnostic strategy for the detection of dystrophin gene mutations in Asian patients and carriers using immortalized cell lines. Journal of Child Neurology 21 (2) : 150-155. ScholarBank@NUS Repository. <a href="https://doi.org/10.1177/08830738060210021101" target="_blank">https://doi.org/10.1177/08830738060210021101</a>
dc.identifier.issn08830738
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/25673
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1177/08830738060210021101
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentPAEDIATRICS
dc.description.doi10.1177/08830738060210021101
dc.description.sourcetitleJournal of Child Neurology
dc.description.volume21
dc.description.issue2
dc.description.page150-155
dc.identifier.isiutNOT_IN_WOS
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