A New Mechanism of Supraventricular Tachycardia: Gene Mutation
SVT has certain genetic characteristics and is often associated with other heart diseases. From the analysis of mutated genes in SVT, it appears to be a type of cardiac ion channel disease. Unlike common ion channel diseases, it is more insidious and more susceptible to external factors. The confirmation of the genetic basis of SVT provides direction for future hazard stratification assessment and gene targeted therapy drug research.
Authors
- Jie Gao (ORCID: https://orcid.org/0000-0001-9579-1703)
- Xiaoping Li (ORCID: https://orcid.org/0000-0002-5057-0226)
- Rong Luo (ORCID: https://orcid.org/0000-0003-3982-8772)
Institutions
- University of Electronic Science and Technology of China (CN)
- Chengdu Medical College (CN)
- Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital (CN)
- Sichuan Provincial Hospital of Traditional Chinese Medicine (CN)
Publication Details
- Journal
- Current Cardiology Reviews
- Published
- 2025-01-22
- DOI
- https://doi.org/10.2174/011573403x320610250108113731
- Primary Topic
- Cardiac Arrhythmias and Treatments
- Type
- article
- Field-Weighted Citation Impact
- 0.00