Impact of ancestral differences and reassessment of the classification of previously reported pathogenic variants in patients with brugada syndrome in the genomic era: A SADS-TW BrS registry

Chen, Ching-Yu JuliusChing-Yu JuliusChenTZU-PIN LULIAN-YU LINYEN BIN LIULI-TING HOHUI-CHUN HUANGLING-PING LAIHWANG, JUEY-JENJUEY-JENHWANGYeh, Shih-Fan SherriShih-Fan SherriYehCHO-KAI WUJYH-MING JIMMY JUANGAntzelevitch, CharlesCharlesAntzelevitch2020-11-172020-11-1720191664-8021https://www.scopus.com/inward/record.uri?eid=2-s2.0-85064216677&doi=10.3389%2ffgene.2018.00680&partnerID=40&md5=c280ce8869c1d2281ab9679f6a21e1f7https://scholars.lib.ntu.edu.tw/handle/123456789/520939English[SDGs]SDG3adult; Article; atrial fibrillation; Brugada syndrome; cohort analysis; controlled study; disease predisposition; DNA extraction; electrocardiography; exome; faintness; family history; female; frameshift mutation; gene frequency; gene mutation; genetic predisposition; genetic variation; genome; genomics; heart death; heart ventricle tachycardia; human; major clinical study; male; middle aged; missense mutation; nonsense mutation; pathogenicity; practice guideline; prevalence; Sanger sequencing; ST segment elevation; thorax painImpact of ancestral differences and reassessment of the classification of previously reported pathogenic variants in patients with brugada syndrome in the genomic era: A SADS-TW BrS registryjournal article10.3389/fgene.2018.006802-s2.0-85064216677