[Clinical and genetic analysis of a Chinese pedigree affected with type 2 Long QT syndrome due to variant of KCNH2 gene].
The KCNH2 gene c.1478A>G (p.Tyr493Cys) variant probably underlay the type 2 LQTS in this pedigree.
Authors
- Haitao Yang (ORCID: https://orcid.org/0000-0002-4987-5794)
- Jintao Wu (ORCID: https://orcid.org/0000-0003-4257-2288)
- Juan Hu (ORCID: https://orcid.org/0000-0002-0175-0167)
- Meng Sun (ORCID: https://orcid.org/0000-0002-7435-3752)
- Jingjing Liu (ORCID: https://orcid.org/0000-0002-6303-8191)
- Lijie Yan (ORCID: https://orcid.org/0000-0003-0966-1799)
- Xiaosheng Chen (ORCID: https://orcid.org/0000-0001-8253-4943)
- Xizheng Xu
Institutions
- Zhengzhou Central Hospital (CN)
Publication Details
- Journal
- PubMed
- Published
- 2024-10-10
- DOI
- https://doi.org/10.3760/cma.j.cn511374-202310100-00179
- Primary Topic
- Cardiac electrophysiology and arrhythmias
- Type
- article