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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Detalles Bibliográficos
Autores principales: Juang, Jyh-Ming Jimmy, Binda, Anna, Lee, Shyh-Jye, Hwang, Juey-Jen, Chen, Wen-Jone, Liu, Yen-Bin, Lin, Lian-Yu, Yu, Chih-Chieh, Ho, Li-Ting, Huang, Hui-Chun, Chen, Ching-Yu Julius, Lu, Tzu-Pin, Lai, Liang-Chuan, Yeh, Shih-Fan Sherri, Lai, Ling-Ping, Chuang, Eric Y., Rivolta, Ilaria, Antzelevitch, Charles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Research paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7341360/
https://www.ncbi.nlm.nih.gov/pubmed/32645615
http://dx.doi.org/10.1016/j.ebiom.2020.102843

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7341360/
https://www.ncbi.nlm.nih.gov/pubmed/32645615
http://dx.doi.org/10.1016/j.ebiom.2020.102843

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