Digenic heterozygous mutations of KCNH2 and SCN5A induced young and early‐onset long QT syndrome and sinoatrial node dysfunction

INTRODUCTION: Long QT syndrome (LQTS) is a life‐threatening inherited channelopathy, and prolonged QT intervals easily trigger malignant arrhythmias, especially torsades de pointes and ventricular fibrillation. MATERIALS AND METHODS: The proband with overlapped phenotypes of LQTS and sinoatrial node...

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Detalles Bibliográficos
Autores principales: Yang, Zhe, Ma, Yuting, Huang, Jiana, Xian, Jianzhong, Huang, Yin, Wu, Linbo, Zhu, WenLiang, Wang, Feng, Chen, Liang, Lin, Xiufang, Lin, Yubi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8739608/
https://www.ncbi.nlm.nih.gov/pubmed/34755423
http://dx.doi.org/10.1111/anec.12889

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8739608/
https://www.ncbi.nlm.nih.gov/pubmed/34755423
http://dx.doi.org/10.1111/anec.12889

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