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Functional characterization of variants in the 5’ UTR and promoter of LDLR gene

dc.contributor.authorAlves, Ana Catarina
dc.contributor.authorMenezes, Juliane
dc.contributor.authorFernandes, Rafael
dc.contributor.authorRomão, Luísa
dc.contributor.authorBourbon, Mafalda
dc.date.accessioned2021-11-11T16:27:29Z
dc.date.available2021-11-11T16:27:29Z
dc.date.issued2021-05
dc.description.abstractBackground and Aims: Familia lhypercholesterolemia (FH) is the most common genetic disorder conferring an increased cardiovascular risk due to cholesterol accumulation since birth. The majority of patients with FH phenotype have mutations in LDLR, APOB or PCSK9 genes. In about 50% of patients a variant causing disease has not been possible to find. The 5'and 3’untranslated regions (UTRs) and promoter of these genes is poorly studied. Consequently, few variants were detected in these locations and functional validation is lacking for the ones described. The aim of this project is to perform an in vitro characterization of variants in 5’UTR and promoter of LDLR gene.pt_PT
dc.description.versionN/Apt_PT
dc.identifier.urihttp://hdl.handle.net/10400.18/7812
dc.language.isoengpt_PT
dc.publisherInstituto Nacional de Saúde Doutor Ricardo Jorge, IPpt_PT
dc.subjectFamilial Hypercholesterolemiapt_PT
dc.subjectCardiovascular Riskpt_PT
dc.subjectDoenças Cardio e Cérebro-vascularespt_PT
dc.subjectDoenças Genéticas
dc.titleFunctional characterization of variants in the 5’ UTR and promoter of LDLR genept_PT
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlace(online)pt_PT
oaire.citation.title89th European Atherosclerosis Society Congress, 30 maio - 2 junho 2021pt_PT
rcaap.rightsembargoedAccesspt_PT
rcaap.typeconferenceObjectpt_PT

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