KCNH2 mutation c.3099_3112del causes congenital long QT syndrome type 2 with gender differences-Reference-Cited by-同舟云学术

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KCNH2 mutation c.3099_3112del causes congenital long QT syndrome type 2 with gender differences

Published:2023-01 Issue: Volume:78 Page:100285
ISSN:1807-5932
Container-title:Clinics
language:en
Short-container-title:Clinics

Author:

Ke ZunPing,Li Chao,Bai Gang,Tan Li,Wang JunFeng,Zhou Ming,Zhou JianHua,Chen Shi-You^ORCID,Dong Xiao^ORCID

Publisher

Elsevier BV

Subject

General Medicine

Reference20 articles.

1. Impact of genetics on the clinical management of channelopathies;Schwartz;J Am Coll Cardiol,2013

2. Long QT syndrome: genetics and future perspective;Wallace;Pediatr Cardiol,2019

3. Genetic testing for long QT syndrome - distinguishing pathogenic mutations from benign variants;Kapa;Circulation,2009

4. QTc: how long is too long?;Johnson;Br J Sports Med,2009

5. Determination and interpretation of the QT interval;Vink;Circulation,2018

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Dofetilide unmasks long QT in a patient presenting with atrial fibrillation–induced cardiomyopathy;HeartRhythm Case Reports;2024-07

2. Exploring the impact of a KCNH2 missense variant on Long QT syndrome: insights into a novel gender-selective, incomplete penetrance inheritance mode;Frontiers in Genetics;2024-05-30

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