Rare Compound Heterozygous Missense Mutation of the <i>SCN5A</i> Gene with Childhood-Onset Sick Sinus Syndrome in Two Chinese Sisters-Reference-Cited by-同舟云学术

Rare Compound Heterozygous Missense Mutation of the <i>SCN5A</i> Gene with Childhood-Onset Sick Sinus Syndrome in Two Chinese Sisters

Published:2023-03-31 Issue:2 Volume:64 Page:299-305
ISSN:1349-2365
Container-title:International Heart Journal
language:en
Short-container-title:Int. Heart J.

Author:

Wang Yanyun¹,Long Siyu²,Wei Chenxi³,Wang Xiaoqin⁴

Affiliation:

1. Laboratory of Molecular Translational Medicine, Center for Translational Medicine, Sichuan University

2. Department of Immunology, West China School of Basic Medical Science and Forensic Medicine, Sichuan University

3. Wu Yuzhang Honors College, Sichuan University

4. Department of Pediatric Cardiology, Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Ministry of Education

Publisher

International Heart Journal (Japanese Heart Journal)

Subject

Cardiology and Cardiovascular Medicine,General Medicine

Link

https://www.jstage.jst.go.jp/article/ihj/64/2/64_22-515/_pdf

Reference21 articles.

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3. 3. Zhu YB, Luo JW, Jiang F, Liu G. Genetic analysis of sick sinus syndrome in a family harboring compound CACNA1C and TTN mutations. Mol Med Rep 2018; 17: 7073-80.

4. 4. Dobrzynski H, Boyett MR, Anderson RH. New insights into pacemaker activity: promoting understanding of sick sinus syndrome. Circulation 2007; 115: 1921-32.

5. 5. Adán V, Crown LA. Diagnosis and treatment of sick sinus syndrome. Am Fam Physician 2003; 67: 1725-32.