TUBGCP2 variants cause lissencephaly spectrum disorders: a case report and literature review
Our study expands the genotype of this brain malformation disorder associated with TUBGCP2 variants by presenting the first case of TUBGCP2 variants causing lissencephaly spectrum disorders in China.
Authors
- Miao Yu (ORCID: https://orcid.org/0000-0001-8608-8354)
- Hua Wang (ORCID: https://orcid.org/0000-0002-5728-7714)
- Tao Yu (ORCID: https://orcid.org/0000-0003-1252-3055)
- Xueyan Liu (ORCID: https://orcid.org/0000-0001-6228-2822)
Institutions
- China Medical University (CN)
Publication Details
- Journal
- Frontiers in Pediatrics
- Published
- 2025-02-13
- DOI
- https://doi.org/10.3389/fped.2025.1476390
- Citations
- 1
- Primary Topic
- Genetics and Neurodevelopmental Disorders
- Type
- article
- Field-Weighted Citation Impact
- 1.82