Validation and Disease Risk Assessment of Previously Reported Genome-Wide Genetic Variants Associated With Brugada Syndrome: SADS-TW BrS Registry

BACKGROUND: Brugada syndrome (BrS) is an oligogenic arrhythmic disease with increased risk of sudden cardiac arrest. Several BrS or ECG traits-related single-nucleotide polymorphisms (SNPs) were identified through previous genome-wide association studies in white patients. We aimed to validate these...

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Detalles Bibliográficos
Autores principales: Jimmy Juang, Jyh-Ming, Liu, Yen-Bin, Julius Chen, Ching-Yu, Yu, Qi-You, Chattopadhyay, Amrita, Lin, Lian-Yu, Chen, Wen-Jone, Yu, Chih-Chien, Huang, Hui-Chun, Ho, Li-Ting, Lai, Ling-Ping, Hwang, Juey-Jen, Lin, Ting-Tse, Liao, Min-Tsun, Chen, Jien-Jiun, Sherri Yeh, Shih-Fan, Chuang, Jing-Yuan, Yang, Dun-Hui, Lin, Jiunn-Lee, Lu, Tzu-Pin, Chuang, Eric Y., Ackerman, Michael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7439932/
https://www.ncbi.nlm.nih.gov/pubmed/32490690
http://dx.doi.org/10.1161/CIRCGEN.119.002797

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7439932/
https://www.ncbi.nlm.nih.gov/pubmed/32490690
http://dx.doi.org/10.1161/CIRCGEN.119.002797

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