CORRECTION article
Front. Genet.
Sec. Neurogenomics
Correction: Case Report: Synergistic effects of an ASXL3 mutation and a 15q11.2 BP1-BP2 microdeletion in a severe neurodevelopmental phenotype
Provisionally accepted
- 1Department of Pediatrics, Zhuzhou Clinical College, Jishou University, Zhuzhou, Hunan, China, Zhuzhou, China
- 2Department of Pediatrics, Zhuzhou Central Hospital, Zhuzhou, China
- 3Zhuzhou Central Hospital, Zhuzhou, China
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Keywords: 15q11.2 BP1-BP2 microdeletion, ASXL3, Dual molecular diagnosis, multilocus pathogenic variation, neurodevelopmental disorder
Received: 17 Dec 2025; Accepted: 17 Dec 2025.
Copyright: © 2025 Yang, Xiao, Chen, Chu and GUOHONG. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence:
Mingkai Yang
HU GUOHONG
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