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CORRECTION article

Front. Genet., 09 January 2026

Sec. Neurogenomics

Volume 16 - 2025 | https://doi.org/10.3389/fgene.2025.1769021

Correction: Case Report: Synergistic effects of an ASXL3 mutation and a 15q11.2 BP1-BP2 microdeletion in a severe neurodevelopmental phenotype

This article is a correction to:

  1. Case Report: Synergistic effects of an ASXL3 mutation and a 15q11.2 BP1-BP2 microdeletion in a severe neurodevelopmental phenotype

    1. Read original article
Mingkai Yang,Mingkai Yang1,2Yanfang XiaoYanfang Xiao2Chanjuan ChenChanjuan Chen2Zhou ChuZhou Chu2Guohong Hu, Guohong Hu1,2*
  • 1Department of Pediatrics, Zhuzhou Clinical College, Jishou University, Zhuzhou, Hunan, China
  • 2Department of Pediatrics, Zhuzhou Central Hospital, Zhuzhou, Hunan, China

A Correction on
Case Report: Synergistic effects of an ASXL3 mutation and a 15q11.2 BP1-BP2 microdeletion in a severe neurodevelopmental phenotype

by Yang M, Xiao Y, Chen C, Chu Z and Hu G (2025). Front. Genet. 16:1674158. doi: 10.3389/fgene.2025.1674158

Affiliation “Department of Pediatrics, Zhuzhou Central Hospital, Zhuzhou, Hunan, China” was omitted for authors Yanfang Xiao, Chanjuan Chen and Zhou Chu. This affiliation has now been added for authors Yanfang Xiao, Chanjuan Chen and Zhou Chu.

Authors Yanfang Xiao, Chanjuan Chen and Zhou Chu were erroneously assigned to affiliation “Department of Pediatrics, Zhuzhou Clinical College, Jishou University, Zhuzhou, Hunan, China”. This affiliation has now been removed for authors Yanfang Xiao, Chanjuan Chen and Zhou Chu.

The original article has been updated.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Keywords: dual molecular diagnosis, ASXL3, 15q11.2 BP1-BP2 microdeletion, multilocus pathogenic variation, neurodevelopmental disorder

Citation: Yang M, Xiao Y, Chen C, Chu Z and Hu G (2026) Correction: Case Report: Synergistic effects of an ASXL3 mutation and a 15q11.2 BP1-BP2 microdeletion in a severe neurodevelopmental phenotype. Front. Genet. 16:1769021. doi: 10.3389/fgene.2025.1769021

Received: 17 December 2025; Accepted: 17 December 2025;
Published: 09 January 2026.

Approved by:

Frontiers in Editorial Office, Frontiers Media SA, Switzerland

Copyright © 2026 Yang, Xiao, Chen, Chu and Hu. 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) and the copyright owner(s) 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: Guohong Hu, MjkwMTcxMjE5QHFxLmNvbQ==

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.