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LDLR, APOB and PCSK9 variants associated with Familial hypercholesterolaemia application of ACMG guidelines for variant interpretation

dc.contributor.authorChora, J.R.
dc.contributor.authorMedeiros, A.M.
dc.contributor.authorAlves, A.C.
dc.contributor.authorBourbon, M.
dc.date.accessioned2017-11-03T16:18:48Z
dc.date.available2017-11-03T16:18:48Z
dc.date.issued2017-05-08
dc.description.abstractFamilial hypercholesterolaemia (FH) is an autosomal dominant disorder of lipid metabolism presenting with increased cardiovascular risk. It is caused by functional mutations in LDLR (>90%), APOB (5-10%) and PCSK9 (1-3%). Although more than 1700 variants have been associated with FH, the great majority have not been proved functionally to affect the LDL receptor cycle. The American College of Medical Genetics and Genomics (ACMG) recently published a guideline for variant interpretation in clinical settings. We aimed to classify, following ACMG guidelines, all published variants associated with FH in different databases and individual reports to establish the proportion of variants that lack evidence to support their pathogenicity. A worldwide overview of FH variants has also been performed.pt_PT
dc.description.sponsorshipThis work was partly supported by a grant from Genediag, Exe. JR Chora and AM Medeiros each have a PhD fellowship funded by FCT (SFRH/BD/108503/2015 and SFRH/BD/113017/2015, respectively). AC Alves is funded by Genediag, Exe (“FH genetic diagnosis” - 2015DPS1165).pt_PT
dc.description.versionN/Apt_PT
dc.identifier.urihttp://hdl.handle.net/10400.18/4810
dc.language.isoengpt_PT
dc.publisherInstituto Nacional de Saúde Doutor Ricardo Jorge, IPpt_PT
dc.subjectFamilial Hypercholesterolaemiapt_PT
dc.subjectDoenças Cardio e Cérebro-vascularespt_PT
dc.titleLDLR, APOB and PCSK9 variants associated with Familial hypercholesterolaemia application of ACMG guidelines for variant interpretationpt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceLisboa, Portugalpt_PT
oaire.citation.titleDia do Jovem Investigador do Instituto Nacional de Saúde Doutor Ricardo Jorge, 8 maio 2017pt_PT
rcaap.rightsembargoedAccesspt_PT
rcaap.typeconferenceObjectpt_PT

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