WWOX-related epileptic encephalopathy caused by a novel mutation in the WWOX gene: a case report
The discovery of novel variants has enriched the existing database of <i>WWOX</i> gene variants and may expand the range of clinical options for treating <i>WWOX</i>-related disorders.
Authors
- Dan Feng (ORCID: https://orcid.org/0000-0001-5926-8894)
- Yanjun Song (ORCID: https://orcid.org/0000-0001-5958-7326)
- Li Ye (ORCID: https://orcid.org/0000-0001-7688-4867)
- Fan Wang (ORCID: https://orcid.org/0000-0003-2423-5202)
- Yating Zhang (ORCID: https://orcid.org/0000-0003-2860-7464)
- Dong-Yuan Qin
Institutions
- Lanzhou University Second Hospital (CN)
- Lanzhou University (CN)
Publication Details
- Journal
- Frontiers in Pediatrics
- Published
- 2024-10-02
- DOI
- https://doi.org/10.3389/fped.2024.1453778
- Citations
- 1
- Primary Topic
- Genetics and Neurodevelopmental Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.55
Funders
- Wu Jieping Medical Foundation