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In silico versus in vitro analysis of LDLR mutations

dc.contributor.authorAlves, A.C.
dc.contributor.authorSilva, S.
dc.contributor.authorPatel, D.
dc.contributor.authorMalhó, R.
dc.contributor.authorSoutar, A.K.
dc.contributor.authorBourbon, M.
dc.date.accessioned2012-07-10T12:47:29Z
dc.date.available2012-07-10T12:47:29Z
dc.date.issued2012-05
dc.description.abstractThe LDL receptor (LDLR) is a glycoprotein that mediates binding and internalization of cholesterol-rich lipoproteins from plasma. Mutations in the LDLR gene are the major cause of familial hypercholesterolaemia (FH), which results in impaired catabolism of circulating LDL. This common autosomal inherited metabolism disorder leads to premature atherosclerosis and increased risk of CHD. Many different mutations (currently more than 1300) have been identified in FH patients, but not all give rise to a defective LDLR.por
dc.identifier.urihttp://hdl.handle.net/10400.18/897
dc.language.isoengpor
dc.publisherInstituto Nacional de Saúde Doutor Ricardo Jorge, IPpor
dc.subjectDoenças Cardio e Cérebro-vascularespor
dc.titleIn silico versus in vitro analysis of LDLR mutationspor
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceMilan, Italypor
oaire.citation.title80th European Atherosclerosis Society Congress-EAS, 25-28 May 2012por
rcaap.rightsopenAccesspor
rcaap.typeconferenceObjectpor

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