Human Genetics of Cardiac Arrhythmias
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-031-44087-8_66
Reference139 articles.
1. Adler A, Novelli V, Amin AS, et al. An international, multicentered, evidence-based reappraisal of genes reported to cause congenital long QT syndrome. Circulation. 2020;141:418–28.
2. Hosseini SM, Kim R, Udupa S, et al. Reappraisal of reported genes for sudden arrhythmic death: evidence-based evaluation of gene validity for Brugada syndrome. Circulation. 2018;138:1195–205.
3. Walsh R, Adler A, Amin AS, et al. Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death. Eur Heart J. 2021;43:1500.
4. Mellor GJ, Blom LJ, Groeneveld SA, et al. Familial evaluation in idiopathic ventricular fibrillation: diagnostic yield and significance of J wave syndromes. Circ Arrhythm Electrophysiol. 2021;14:e009089.
5. Neves R, Tester DJ, Simpson MA, et al. Exome sequencing highlights a potential role for concealed cardiomyopathies in youthful sudden cardiac death. Circ Genom Precis Med. 2022;15:e003497.
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