SLC2A1 variants cause late-onset epilepsy and the genetic-dependent stage feature
SLC2A1 variants are associated with late-onset epilepsy, which is consistent with the genetic-dependent stage feature of SLC2A1. Early genetic diagnosis is important for treatment of patients with SLC2A1 variants.
Authors
- Yan Ding (ORCID: https://orcid.org/0000-0002-0136-8275)
- Hao Yan (ORCID: https://orcid.org/0000-0001-7765-7404)
- Bingmei Li
- Dongfang Zou (ORCID: https://orcid.org/0000-0001-6726-8704)
- Lingjuan Fei
- Zi-sheng Lin (ORCID: https://orcid.org/0009-0007-8065-9962)
- Pengyu Wang (ORCID: https://orcid.org/0000-0002-6336-7673)
- Bin Li (ORCID: https://orcid.org/0000-0003-2248-4002)
- Jie Wang (ORCID: https://orcid.org/0000-0002-7002-7247)
- Jiayi Zhong (ORCID: https://orcid.org/0009-0008-7372-0697)
- Dongming Zhang (ORCID: https://orcid.org/0000-0001-7175-1811)
- Kai Peng (ORCID: https://orcid.org/0000-0001-9901-6448)
- Wei‐Ping Liao (ORCID: https://orcid.org/0000-0001-9929-9185)
- Sheng Luo (ORCID: https://orcid.org/0000-0002-7184-1267)
- Ye Hong (ORCID: https://orcid.org/0000-0002-5014-5027)
- Qiong‐Xiang Zhai (ORCID: https://orcid.org/0000-0001-6526-4398)
- Jing Guo (ORCID: https://orcid.org/0009-0005-8497-9758)
Institutions
- Guangdong General Hospital (CN)
- Second Affiliated Hospital of Guangzhou Medical University (CN)
- First People's Hospital of Foshan (CN)
- Guangdong Academy of Medical Sciences (CN)
- Shenzhen Children's Hospital (CN)
- First Affiliated Hospital of Jinan University (CN)
- Guangdong 999 Brain Hospital (CN)
- Guangzhou Medical University (CN)
Publication Details
- Journal
- Acta Epileptologica
- Published
- 2024-11-07
- DOI
- https://doi.org/10.1186/s42494-024-00177-0
- Citations
- 6
- Primary Topic
- Genomics and Rare Diseases
- Type
- article
- Field-Weighted Citation Impact
- 3.30
Funders
- National Natural Science Foundation of China
- UCB Pharma