Publication
Criteria to predict carriers of a novel SCN5A mutation in a large Portuguese family affected by the Brugada syndrome
dc.contributor.author | Santos, L. F. | |
dc.contributor.author | Rodrigues, B. | |
dc.contributor.author | Moreira, D. | |
dc.contributor.author | Correia, E. | |
dc.contributor.author | Nunes, L. | |
dc.contributor.author | Costa, A. | |
dc.contributor.author | Elvas, L. | |
dc.contributor.author | Pereira, T. | |
dc.contributor.author | Machado, J. C. | |
dc.contributor.author | Castedo, S. | |
dc.contributor.author | Henriques, C. | |
dc.contributor.author | Matos, A. | |
dc.contributor.author | Santos, J. O. | |
dc.date.accessioned | 2017-02-03T08:42:21Z | |
dc.date.available | 2017-02-03T08:42:21Z | |
dc.date.issued | 2012 | |
dc.description.abstract | Brugada syndrome (BrS) is a life-threatening arrhythmia disorder associated with autosomal-dominant mutations in the SCN5A gene. We aimed to characterize the diagnostic challenges and clinical manifestations of a novel SCN5A mutation associated with BrS. | pt_PT |
dc.description.version | info:eu-repo/semantics/publishedVersion | pt_PT |
dc.identifier.citation | Santos, L. F., Rodrigues, B., Moreira, D., Correia, E., Nunes, L., Costa, A., Elvas, L., Pereira, T., Machado, J. C., Henriques, C., Matos, A. & Santos, J. O. (2012). Criteria to predict carriers of a novel SCN5A mutation in a large Portuguese family affected by the Brugada syndrome. Europace, 14(6), 882–8 | pt_PT |
dc.identifier.doi | 10.1093/europace/eur421 | pt_PT |
dc.identifier.uri | http://hdl.handle.net/10400.19/4382 | |
dc.language.iso | eng | pt_PT |
dc.peerreviewed | yes | pt_PT |
dc.relation.publisherversion | https://academic.oup.com/europace/article/14/6/882/547744/Criteria-to-predict-carriers-of-a-novel-SCN5A | pt_PT |
dc.subject | Brugada Syndrome | pt_PT |
dc.subject | SCN5A mutation | pt_PT |
dc.subject | ECG | pt_PT |
dc.subject | SAECG | pt_PT |
dc.subject | Diagnostic criteria | pt_PT |
dc.subject | Sudden cardiac death | pt_PT |
dc.title | Criteria to predict carriers of a novel SCN5A mutation in a large Portuguese family affected by the Brugada syndrome | pt_PT |
dc.type | journal article | |
dspace.entity.type | Publication | |
oaire.citation.endPage | 888 | pt_PT |
oaire.citation.issue | 6 | pt_PT |
oaire.citation.startPage | 882 | pt_PT |
oaire.citation.title | Europace | pt_PT |
oaire.citation.volume | 14 | pt_PT |
rcaap.rights | openAccess | pt_PT |
rcaap.type | article | pt_PT |