Malignant Arrhythmogenic Role Associated with RBM20: A Comprehensive Interpretation Focused on a Personalized Approach

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.authorCésar Diaz, Sergio
dc.contributor.authorTiron, Coloma
dc.contributor.authorIglesias, Anna
dc.contributor.authorBrugada Terradellas, Josep, 1958-
dc.contributor.authorBrugada, Ramon
dc.contributor.authorCampuzano Larrea, Oscar
dc.date.accessioned2021-04-07T07:56:08Z
dc.date.available2021-04-07T07:56:08Z
dc.date.issued2021-02-15
dc.date.updated2021-03-25T08:24:01Z
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.identifier.pmid33671899
dc.identifier.urihttps://hdl.handle.net/2445/176024
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.accessRightsinfo:eu-repo/semantics/openAccess
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

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