Compound heterozygous SCN5A gene mutations in asymptomatic Brugada syndrome child-Reference-Cited by-同舟云学术

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Compound heterozygous SCN5A gene mutations in asymptomatic Brugada syndrome child

Published:2012-09-17 Issue:1 Volume:2 Page:11
ISSN:2035-8148
Container-title:Cardiogenetics
language:
Short-container-title:Cardiogenetics

Author:

Sommariva Elena,Vatta Matteo,Xi Yutao,Sala Simone,Ai Tomohiko,Cheng Jie,Pappone Carlo,Ferrari Maurizio,Benedetti Sara

Publisher

MDPI AG

Subject

General Earth and Planetary Sciences,General Environmental Science

Link

http://www.pagepressjournals.org/index.php/cardiogen/article/viewFile/504/pdf

Cited by 4 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. Atrial standstill in the newborn: a case report;Russian Journal of Cardiology;2021-08-08

2. β1 and β3 subunits amplify mechanosensitivity of the cardiac voltage-gated sodium channel Nav1.5;Pflügers Archiv - European Journal of Physiology;2019-11-14

3. Irritable bowel syndrome patients have SCN5A channelopathies that lead to decreased NaV1.5 current and mechanosensitivity;American Journal of Physiology-Gastrointestinal and Liver Physiology;2018-04-01

4. Genetics can contribute to the prognosis of Brugada syndrome: a pilot model for risk stratification;European Journal of Human Genetics;2013-01-16

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