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LDLR functional in vitro assays: a step forward for the correct genetic diagnosis of familial hypercholesterolemia

dc.contributor.authorAzevedo, S.
dc.contributor.authorAlves, A.C.
dc.contributor.authorMedeiros, A.M.
dc.contributor.authorBarros, P.
dc.contributor.authorMartín, C.
dc.contributor.authorBourbon, M.
dc.date.accessioned2015-06-26T10:52:12Z
dc.date.available2015-06-26T10:52:12Z
dc.date.issued2015-06
dc.description.abstractAim: Familial hypercholesterolaemia (FH) is an autosomal dominant disorder that confers an increased cardiovascular risk, due to high levels of cholesterol in blood since birth. FH has a prevalence of 1:500 and about 90% of these patients have mutations in the LDLR. Although more than 1600 alterations have been identified in FH patients, the majority of them remain without functional studies, being the aim of this work to construct vectors for the in vitro study of common alterations in Portuguese FH patients, contributing for phenotype/genotype clarification.por
dc.identifier.urihttp://hdl.handle.net/10400.18/3065
dc.language.isoengpor
dc.publisherInstituto Nacional de Saúde Doutor Ricardo Jorge, IPpor
dc.subjectDoenças Cardio e Cérebro-vascularespor
dc.subjectFamilial Hypercholesterolaemiapor
dc.titleLDLR functional in vitro assays: a step forward for the correct genetic diagnosis of familial hypercholesterolemiapor
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceGlasgow, United Kingdompor
oaire.citation.titleEuropean Society of Human Genetics Conference 2015, June 6-9, 2015por
rcaap.rightsembargoedAccesspor
rcaap.typeconferenceObjectpor

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