Mutation analysis in a small cohort of New Zealand patients originating from the United Kingdom demonstrates genetic heterogeneity in familial hypercholestorolemia

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dc.contributor.authorThiart R
dc.contributor.authorVarret M
dc.contributor.authorLintott CJ
dc.contributor.authorScott RS
dc.contributor.authorLoubser L
dc.contributor.authorDu Plessis L
dc.contributor.authorDe Villiers JNP
dc.contributor.authorBoileau C
dc.contributor.authorKotze MJ
dc.date.accessioned2013-01-23T10:10:34Z
dc.date.available2013-01-23T10:10:34Z
dc.date.issued2000
dc.descriptionGesondheidswetenskappe
dc.descriptionVerloskunde En Ginekologie
dc.descriptionPlease help us populate SUNScholar with the post print version of this article. It can be e-mailed to: scholar@sun.ac.za
dc.identifier.citationMolecular and Cellular Probes
dc.identifier.urihttp://hdl.handle.net/10019.1/72260
dc.publisherACADEMIC PRESS LTD ELSEVIER SCIENCE LTD, 24-28 OVAL RD, LONDON, ENGLAND, NW17DX
dc.titleMutation analysis in a small cohort of New Zealand patients originating from the United Kingdom demonstrates genetic heterogeneity in familial hypercholestorolemia
dc.typeJournal Articles (subsidised)
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