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Genomic characterization in dilated cardiomyopathy

dc.contributor.authorCosta, Marina C.
dc.date.accessioned2019-07-26T15:26:12Z
dc.date.available2019-07-26T15:26:12Z
dc.date.issued2019
dc.description© 2019 Sociedade Portuguesa de Cardiologia. Published by Elsevier España, S.L.U. All rights reserved.pt_PT
dc.description.abstractDilated cardiomyopathy (DCM), a leading cause of heart failure and sudden cardiac death, is characterized by ventricular dilatation and impaired systolic function in the absence of abnormal loading conditions or coronary artery disease. Its prevalence is approximately 1 in 2500 individuals, and 30-50% of cases are familial.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationRev Port Cardiol. 2019;38(6):449-450pt_PT
dc.identifier.doi10.1016/j.repc.2019.02.006pt_PT
dc.identifier.issn0870-2551
dc.identifier.urihttp://hdl.handle.net/10451/39249
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherElesevierpt_PT
dc.relation.publisherversionhttps://www.sciencedirect.com/journal/revista-portuguesa-de-cardiologiapt_PT
dc.titleGenomic characterization in dilated cardiomyopathypt_PT
dc.title.alternativeCaracterização genómica na cardiomiopatia dilatadapt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage450pt_PT
oaire.citation.issue6pt_PT
oaire.citation.startPage449pt_PT
oaire.citation.titleRevista Portuguesa de Cardiologíapt_PT
oaire.citation.volume38pt_PT
person.familyNameCosta
person.givenNameMarina
person.identifier.ciencia-id6818-7810-6CEC
person.identifier.orcid0000-0001-9020-7539
person.identifier.ridO-1710-2014
person.identifier.scopus-author-id55453276400
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
relation.isAuthorOfPublicationc4dcab9e-b873-4587-bb30-5203af150404
relation.isAuthorOfPublication.latestForDiscoveryc4dcab9e-b873-4587-bb30-5203af150404

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