GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death

GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death

Background: Brugada syndrome (BrS) is a rare inherited disease causing sudden cardiac death (SCD). Copy number variants (CNVs) can contribute to disease susceptibility, but their role in Brugada syndrome (BrS) is unknown. We aimed to identify a CNV associated with BrS and elucidated its clinical imp...

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Bibliographic Details
Main Authors: Jyh-Ming Jimmy Juang, Anna Binda, Shyh-Jye Lee, Juey-Jen Hwang, Wen-Jone Chen, Yen-Bin Liu, Lian-Yu Lin, Chih-Chieh Yu, Li-Ting Ho, Hui-Chun Huang, Ching-Yu Julius Chen, Tzu-Pin Lu, Liang-Chuan Lai, Shih-Fan Sherri Yeh, Ling-Ping Lai, Eric Y. Chuang, Ilaria Rivolta, Charles Antzelevitch
Format: Article
Language:English
Published: Elsevier 2020-07-01
Series:EBioMedicine
Subjects:
Inherited cardiac arrhythmia
Genetics
Sudden cardiac death
Brugada syndrome
Online Access:http://www.sciencedirect.com/science/article/pii/S2352396420302188

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http://www.sciencedirect.com/science/article/pii/S2352396420302188

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