Identification of a SCN5A founder mutation causing sudden death, Brugada syndrome, and conduction blocks in Southern Italy-Reference-Cited by-同舟云学术

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Identification of a SCN5A founder mutation causing sudden death, Brugada syndrome, and conduction blocks in Southern Italy

Published:2021-10 Issue:10 Volume:18 Page:1698-1706
ISSN:1547-5271
Container-title:Heart Rhythm
language:en
Short-container-title:Heart Rhythm

Author:

Curcio Antonio,Malovini Alberto,Mazzanti Andrea,Memmi Mirella,Gambelli Patrick,La Rosa Francesca,Bloise Raffaella,Indolfi Ciro,Bellazzi Riccardo,Napolitano Carlo

Funder

Ministero della Salute

Publisher

Elsevier BV

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference28 articles.

1. Using population isolates in genetic association studies;Hatzikotoulas;Brief Funct Genomics,2014

2. Reappraisal of reported genes for sudden arrhythmic death: evidence-based evaluation of gene validity for Brugada syndrome;Hosseini;Circulation,2018

3. Genetics of sudden cardiac death;Bezzina;Circ Res,2015

4. Polymorphisms in the NOS1AP gene modulate QT interval duration and risk of arrhythmias in the Long QT Syndrome;Tomas;J Am Coll Cardiol,2010

5. Founder mutations in the Netherlands: SCN5a 1795insD, the first described arrhythmia overlap syndrome and one of the largest and best characterised families worldwide;Postema;Neth Heart J,2009

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. Pathophysiology of Atrial Fibrillation and Approach to Therapy in Subjects Less than 60 Years Old;International Journal of Molecular Sciences;2024-01-07

2. The genomic architecture of the Brugada syndrome;Heart Rhythm;2021-10

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