A 59-Year-Old Woman with Familial Brugada Syndrome and the c.664C>T Variant of the Sodium Voltage-Gated Channel Alpha Subunit 5 (SCN5A) Gene, Accompanied by Congenital Absence of the Right Coronary Artery, Patent Foramen Ovale, and Ischemic Stroke-Reference-Cited by-同舟云学术

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A 59-Year-Old Woman with Familial Brugada Syndrome and the c.664C>T Variant of the Sodium Voltage-Gated Channel Alpha Subunit 5 (SCN5A) Gene, Accompanied by Congenital Absence of the Right Coronary Artery, Patent Foramen Ovale, and Ischemic Stroke

Published:2021-08-12 Issue: Volume:22 Page:
ISSN:1941-5923
Container-title:American Journal of Case Reports
language:en
Short-container-title:Am J Case Rep

Author:

Katsaras Dimitrios¹,Sanjeev Kumar Bangalore Thimmappa²,Patel Billal¹,Chalil Shajil¹,Abozguia Khalid¹

Affiliation:

1. Department of Cardiology, Lancashire Cardiac Centre, Blackpool Teaching Hospitals NHS Foundation Trust, Blackpool, United Kingdom

2. Department of Radiology, Blackpool Teaching Hospitals NHS Foundation Trust, Blackpool, United Kingdom

Publisher

International Scientific Information, Inc.

Subject

General Medicine

Cited by 3 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. Relationship Between Brugada Syndrome and Ischemic Stroke: A Case Report and Comprehensive Literature Review;American Journal of Case Reports;2024-04-05

2. Polymorphic Variants of SCN5A Gene (rs41312433 and rs1805124) Associated with Coronary Artery Affliction in Patients with Severe Arrhythmias;Genes;2024-02-02

3. Single coronary artery presenting dilated cardiomyopathy and hyperlipidemia with the SCN5A and APOA5 gene mutation: A case report and review of the literature;Frontiers in Cardiovascular Medicine;2023-05-22

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