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In silico classification of LDLR variants leads to misdiagnosis of FH patients – validation of a novel criteria

dc.contributor.authorAlves, Ana Catarina
dc.contributor.authorMedeiros, Ana Margarida
dc.contributor.authorBourbon, Mafalda
dc.date.accessioned2014-10-30T17:18:34Z
dc.date.available2014-10-30T17:18:34Z
dc.date.issued2014-05
dc.description.abstractIntrodution: Familial Hypercholesterolaemia (FH) is a genetic disorder most commonly caused by mutations in LDLR gene. More than 1300 different mutations on LDLR gene have been described as causing FH but, as has been previously shown, the simple finding of a variation in the coding sequence of the LDLR does not determine the actual cause of FH. Functional assessment is necessary to prove pathogenicity. The aim of this study was to compare results of in silico and in vitro functional analysis of 40 alterations in LDLR and with that validate an in silico model.por
dc.description.sponsorshipProject grants Science and Technology Foundation [PTDC/SAU-GMG/101874/2008] and Strategic Project Grant [PEst-OE/BIA/UI4046/2011].por
dc.identifier.urihttp://hdl.handle.net/10400.18/2439
dc.language.isoengpor
dc.publisherInstituto Nacional de Saúde Doutor Ricardo Jorge, IPpor
dc.subjectDoenças Cardio e Cérebro-vascularespor
dc.subjectFamilial Hypercholesterolaemia (por
dc.titleIn silico classification of LDLR variants leads to misdiagnosis of FH patients – validation of a novel criteriapor
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceMadrid, Espanhapor
oaire.citation.titleEuropean Atherosclerosis Congress, 31 May - 3 June, 2014por
rcaap.rightsembargoedAccesspor
rcaap.typeconferenceObjectpor

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