A Novel Variant in SLC4A3 Gene Mutation Associated With Familial Short QT Syndrome and Sudden Death
This report describes a previously unreported SLC4A3 variant associated with familial SQTS and sudden death, reinforcing the gene's pathogenic role.
Authors
- Letteria Bruno
- Antonino Micari (ORCID: https://orcid.org/0000-0003-4165-6439)
- Pasquale Crea (ORCID: https://orcid.org/0000-0002-0645-8579)
- Francesco De Luca (ORCID: https://orcid.org/0000-0002-5878-6240)
- Carla Giustetto (ORCID: https://orcid.org/0000-0002-5102-3398)
- Lilia Oreto (ORCID: https://orcid.org/0000-0002-3606-1812)
Institutions
- University of Messina (IT)
- Azienda Ospedaliera Citta' della Salute e della Scienza di Torino (IT)
- University of Turin (IT)
Publication Details
- Journal
- Journal of Cardiovascular Electrophysiology
- Published
- 2025-10-02
- DOI
- https://doi.org/10.1111/jce.70126
- Citations
- 1
- Primary Topic
- Cardiac electrophysiology and arrhythmias
- Type
- article
- Field-Weighted Citation Impact
- 1.39