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Improving Familial Hypercholesterolaemia Diagnosis – Functional in Vitro Analysis of LDLR Missense Variants Found in the Portuguese FH Cohort

dc.contributor.authorAlves, Ana C.
dc.contributor.authorGraça, Rafael
dc.contributor.authorBourbon, Mafalda
dc.date.accessioned2019-04-01T16:27:09Z
dc.date.available2019-04-01T16:27:09Z
dc.date.issued2018-06
dc.description.abstractObjective: Familial Hypercholesterolaemia (FH) is an autosomal disorder of lipid metabolism presenting with increased cardiovascular risk due to lifelong exposure to high LDL values. LDLR mutations are the cause of disease in 90% of the cases but proof of pathogenicity has only been obtained for about 10%. The lack of functional characterization of variants found in patients with a clinical diagnosis of FH makes it difficult to reach a definite FH diagnosis.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationAtherosclerosis.2018 Jun;32(Suppl.):54pt_PT
dc.identifier.doi10.1016/j.atherosclerosissup.2018.04.162pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.18/6357
dc.language.isoengpt_PT
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S1567568818301624?via%3Dihubpt_PT
dc.subjectFamilial Hypercholesterolaemiapt_PT
dc.subjectDoenças Cardio e Cérebro-vascularespt_PT
dc.titleImproving Familial Hypercholesterolaemia Diagnosis – Functional in Vitro Analysis of LDLR Missense Variants Found in the Portuguese FH Cohortpt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceToronto, Canadápt_PT
oaire.citation.startPage54pt_PT
oaire.citation.titleInternational Symposium on Atherosclerosis (ISA), 9-12 Jun 2018pt_PT
oaire.citation.volume32pt_PT
rcaap.rightsembargoedAccesspt_PT
rcaap.typeconferenceObjectpt_PT

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