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Editorial to "Atrial standstill in a young patient with ischemic stroke associated with inheritance of a novel HCN4 mutation".

作者信息

Kondo Hidekazu, Takahashi Naohiko

机构信息

Department of Cardiology and Clinical Examination, Faculty of Medicine Oita University Yufu Oita Japan.

出版信息

J Arrhythm. 2024 Oct 7;40(6):1523-1524. doi: 10.1002/joa3.13164. eCollection 2024 Dec.

DOI:10.1002/joa3.13164
PMID:39669920
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11632256/
Abstract
摘要

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Editorial to "Atrial standstill in a young patient with ischemic stroke associated with inheritance of a novel HCN4 mutation".《关于“一名患有缺血性中风的年轻患者出现心房停搏,与一种新的HCN4突变遗传相关”的社论》
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2
Atrial standstill in a young patient with ischemic stroke associated with inheritance of a novel HCN4 mutation.一名年轻的缺血性中风患者出现心房停搏,与一种新的HCN4突变遗传有关。
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本文引用的文献

1
Sick sinus syndrome with HCN4 mutations shows early onset and frequent association with atrial fibrillation and left ventricular noncompaction.伴有HCN4基因突变的病态窦房结综合征发病早,且常与心房颤动和左心室心肌致密化不全相关。
Heart Rhythm. 2017 May;14(5):717-724. doi: 10.1016/j.hrthm.2017.01.020. Epub 2017 Jan 17.
2
Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type I.靶向重测序确定TRPM4是导致I型进行性家族性心脏传导阻滞的主要易感基因。
Int J Cardiol. 2016 Mar 15;207:349-58. doi: 10.1016/j.ijcard.2016.01.052. Epub 2016 Jan 11.
3
Novel mutation in the α-myosin heavy chain gene is associated with sick sinus syndrome.一种新的α-肌球蛋白重链基因突变与病态窦房结综合征有关。
Circ Arrhythm Electrophysiol. 2015 Apr;8(2):400-8. doi: 10.1161/CIRCEP.114.002534. Epub 2015 Feb 25.
4
Natural history of dilated cardiomyopathy due to lamin A/C gene mutations.由核纤层蛋白A/C基因突变引起的扩张型心肌病的自然病史。
J Am Coll Cardiol. 2003 Mar 5;41(5):771-80. doi: 10.1016/s0735-1097(02)02954-6.