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1
Cardiac conduction defects.心脏传导缺陷
Acta Biomed. 2019 Sep 30;90(10-S):20-29. doi: 10.23750/abm.v90i10-S.8751.
2
p.N1380del mutation in the pore-forming region of SCN5A gene is associated with cardiac conduction disturbance and ventricular tachycardia.SCN5A 基因突变位于通道形成区，与心脏传导障碍和室性心动过速有关。
Acta Biochim Biophys Sin (Shanghai). 2017 Mar 1;49(3):270-276. doi: 10.1093/abbs/gmx003.
3
Case reports of a c.475G>T, p.E159* lamin A/C mutation with a family history of conduction disorder, dilated cardiomyopathy and sudden cardiac death.携带c.475G>T、p.E159*型核纤层蛋白A/C突变且有传导障碍、扩张型心肌病和心源性猝死家族史的病例报告。
BMC Cardiovasc Disord. 2019 Dec 17;19(1):298. doi: 10.1186/s12872-019-01282-6.
4
Emerging Implications of Genetic Testing in Inherited Primary Arrhythmia Syndromes.基因检测在遗传性原发性心律失常综合征中的新影响
Cardiol Rev. 2019 Jan/Feb;27(1):23-33. doi: 10.1097/CRD.0000000000000203.
5
Familial Clustering of Cardiac Conduction Defects and Pacemaker Insertion.家族性心脏传导缺陷和起搏器植入的聚集性。
Circ Arrhythm Electrophysiol. 2019 Jul;12(7):e007150. doi: 10.1161/CIRCEP.119.007150. Epub 2019 Jun 20.
6
Molecular and genetic insights into progressive cardiac conduction disease.渐进性心脏传导疾病的分子和遗传见解。
Europace. 2019 Aug 1;21(8):1145-1158. doi: 10.1093/europace/euz109.
7
A Novel Familial Cardiac Arrhythmia Syndrome with Widespread ST-Segment Depression.一种伴有广泛ST段压低的新型家族性心律失常综合征。
N Engl J Med. 2018 Nov 1;379(18):1780-1781. doi: 10.1056/NEJMc1807668.
8
Evaluation and Treatment of Patients With Bradycardia and Cardiac Conduction Delay: Recommendations for Permanent Pacing.
JAMA Cardiol. 2019 Aug 1;4(8):823-824. doi: 10.1001/jamacardio.2019.1231.
9
Mutation in Patients With Ventricular Noncompaction and Cardiac Conduction Disease.心室致密化不全与心脏传导疾病患者的突变
Circ Genom Precis Med. 2018 May;11(5):e002103. doi: 10.1161/CIRCGEN.118.002103.
10
Ventricular tachycardia in the absence of structural heart disease.无结构性心脏病的室性心动过速。
Heart. 2019 Apr;105(8):645-656. doi: 10.1136/heartjnl-2017-311590. Epub 2018 Dec 12.
引用本文的文献
1
[Molecular autopsy: post-mortem genetic testing following sudden cardiac death].[分子尸检：心脏性猝死后的尸检基因检测]
Inn Med (Heidelb). 2025 Jul 11. doi: 10.1007/s00108-025-01934-0.
2
Human Genetics of Cardiac Arrhythmias.心律失常的人类遗传学。
Adv Exp Med Biol. 2024;1441:1033-1055. doi: 10.1007/978-3-031-44087-8_66.
本文引用的文献
1
TRPM4 mutations to cause autosomal recessive and not autosomal dominant Brugada type 1 syndrome.TRPM4突变导致常染色体隐性而非常染色体显性1型Brugada综合征。
Eur J Med Genet. 2019 Jun;62(6):103527. doi: 10.1016/j.ejmg.2018.08.008. Epub 2018 Aug 22.
2
Atrial Fibrillation: Epidemiology, Pathophysiology, and Clinical Outcomes.心房颤动：流行病学、病理生理学及临床结局
Circ Res. 2017 Apr 28;120(9):1501-1517. doi: 10.1161/CIRCRESAHA.117.309732.
3
Atrioventricular Accessory Pathways: Mechanisms, Electrocardiograms, and Associated Arrhythmias.房室旁路：机制、心电图及相关心律失常
South Med J. 2016 Oct;109(10):670-676. doi: 10.14423/SMJ.0000000000000538.
4
2016 ESC Guidelines for the management of atrial fibrillation developed in collaboration with EACTS.2016年欧洲心脏病学会（ESC）与欧洲心胸外科学会（EACTS）合作制定的心房颤动管理指南。
Eur Heart J. 2016 Oct 7;37(38):2893-2962. doi: 10.1093/eurheartj/ehw210. Epub 2016 Aug 27.
5
Inherited ion channel diseases: a brief review.遗传性离子通道疾病：简要综述。
Europace. 2015 Oct;17 Suppl 2:ii1-6. doi: 10.1093/europace/euv105.
6
Short QT Syndrome - Review of Diagnosis and Treatment.短QT综合征——诊断与治疗综述
Arrhythm Electrophysiol Rev. 2014 Aug;3(2):76-9. doi: 10.15420/aer.2014.3.2.76. Epub 2014 Aug 30.
7
The prevalence and significance of a short QT interval in 18,825 low-risk individuals including athletes.在包括运动员在内的 18825 名低危个体中，短 QT 间期的发生率和意义。
Br J Sports Med. 2016 Jan;50(2):124-9. doi: 10.1136/bjsports-2015-094827. Epub 2015 Sep 23.
8
CALM3 mutation associated with long QT syndrome.与长QT综合征相关的CALM3突变。
Heart Rhythm. 2015 Feb;12(2):419-22. doi: 10.1016/j.hrthm.2014.10.035. Epub 2014 Oct 31.
9
Genetics of long QT syndrome.长QT综合征的遗传学
Methodist Debakey Cardiovasc J. 2014 Jan-Mar;10(1):29-33. doi: 10.14797/mdcj-10-1-29.
10
Genotype- and phenotype-guided management of congenital long QT syndrome.基于基因型和表型的先天性长 QT 综合征管理。
Curr Probl Cardiol. 2013 Oct;38(10):417-55. doi: 10.1016/j.cpcardiol.2013.08.001.
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