Roles of Single Nucleotide Polymorphisms in the SLC6A2 Gene in the Risk of Vasovagal Syncope Among Children in Eastern China: A Case‐Control Study

Roles of Single Nucleotide Polymorphisms in the SLC6A2 Gene in the Risk of Vasovagal Syncope Among Children in Eastern China: A Case‐Control Study

ABSTRACT Background and Aims Vasovagal syncope (VVS) is a primary reason for fainting in children, affected by numerous genetic and environmental factors. We designed this study to investigate the impact of SLC6A2 gene polymorphisms and gene‐environment interactions on the etiology of VVS in childre...

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Bibliographic Details
Main Authors: Minmin Wang, Meng Li, Haizhao Zhao, Xiaoyue Liu, Qingyu Kong, Cuifen Zhao, Baomin Li
Format: Article
Language:English
Published: Wiley 2025-03-01
Series:Health Science Reports
Subjects:
children
etiology
SLC6A2
vasovagal syncope
Online Access:https://doi.org/10.1002/hsr2.70585
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