Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/176024
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dc.contributor.authorJordà Burgos, Paloma-
dc.contributor.authorToro, Rocío-
dc.contributor.authorDiez, Carles-
dc.contributor.authorSalazar Mendiguchía, Joel-
dc.contributor.authorFernández Falgueras, Anna-
dc.contributor.authorPérez Serra, Alexandra-
dc.contributor.authorColl, Mònica-
dc.contributor.authorPuigmulé, Marta-
dc.contributor.authorArbelo, Elena-
dc.contributor.authorGarcía Álvarez, Ana-
dc.contributor.authorSarquella Brugada, Georgia-
dc.contributor.authorCesar, Sergi-
dc.contributor.authorTiron, Coloma-
dc.contributor.authorIglesias, Anna-
dc.contributor.authorBrugada Terradellas, Josep, 1958--
dc.contributor.authorBrugada, Ramon-
dc.contributor.authorCampuzano, Òscar-
dc.date.accessioned2021-04-07T07:56:08Z-
dc.date.available2021-04-07T07:56:08Z-
dc.date.issued2021-02-15-
dc.identifier.urihttp://hdl.handle.net/2445/176024-
dc.description.abstractThe RBM20 gene encodes the muscle-specific splicing factor RNA-binding motif 20, a regulator of heart-specific alternative splicing. Nearly 40 potentially deleterious variants in RBM20 have been reported in the last ten years, being found to be associated with highly arrhythmogenic events in familial dilated cardiomyopathy. Frequently, malignant arrhythmias can be a primary manifestation of disease. The early recognition of arrhythmic genotypes is crucial in avoiding lethal episodes, as it may have an impact on the adoption of personalized preventive measures. Our study performs a comprehensive update of data concerning rare variants in RBM20 that are associated with malignant arrhythmogenic phenotypes with a focus on personalized medicine.-
dc.format.extent17 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherMDPI-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.3390/jpm11020130-
dc.relation.ispartofJournal of Personalized Medicine, 2021, vol. 11, num. 2-
dc.relation.urihttps://doi.org/10.3390/jpm11020130-
dc.rightscc by (c) Jordà et al., 2021-
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))-
dc.subject.classificationArrítmia-
dc.subject.classificationAturada cardíaca-
dc.subject.classificationGenètica-
dc.subject.otherArrhythmia-
dc.subject.otherCardiac arrest-
dc.subject.otherGenetics-
dc.titleMalignant Arrhythmogenic Role Associated with RBM20: A Comprehensive Interpretation Focused on a Personalized Approach-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.date.updated2021-03-25T08:24:01Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid33671899-
Appears in Collections:Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)
Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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