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CORRECTION article

Front. Genet., 07 November 2025

Sec. Genetics of Common and Rare Diseases

Volume 16 - 2025 | https://doi.org/10.3389/fgene.2025.1722189

Correction: A novel splicing variant in NBAS identified by minigene assay causes infantile liver failure syndrome type 2

This article is a correction to:

  1. A novel splicing variant in NBAS identified by minigene assay causes infantile liver failure syndrome type 2

    1. Read original article
Anna HuAnna Hu1Jun LiangJun Liang1Hongbo LiuHongbo Liu1Jinghui JiangJinghui Jiang1Fujing XieFujing Xie1Xin Zhou Xin Zhou2*Xiaojia Zhang Xiaojia Zhang1*
  • 1Department of Pediatrics, Liaocheng People’s Hospital, Liaocheng, China
  • 2Department of Cardiology, Children’s Hospital Affiliated to Shandong University (Jinan Children’s Hospital), Jinan, China

A Correction on
A novel splicing variant in NBAS identified by minigene assay causes infantile liver failure syndrome type 2

by Hu A, Liang J, Liu H, Jiang J, Xie F, Zhou X and Zhang X (2025). Front. Genet. 16:1687266. doi: 10.3389/fgene.2025.1687266

The order of authors in the author list of the published paper was erroneously given as: Anna Hu1, Jun Liang1, Hongbo Liu1, Jinghui Jiang1, Fujing Xie1, Xiaojia Zhang1* and Xin Zhou2*.

The correct author list reads:

Anna Hu1, Jun Liang1, Hongbo Liu1, Jinghui Jiang1, Fujing Xie1, Xin Zhou2* and Xiaojia Zhang1*.

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: NBAS, ILFS2, splicing variant, minigene assay, whole-exome sequencing, acute liver failure

Citation: Hu A, Liang J, Liu H, Jiang J, Xie F, Zhou X and Zhang X (2025) Correction: A novel splicing variant in NBAS identified by minigene assay causes infantile liver failure syndrome type 2. Front. Genet. 16:1722189. doi: 10.3389/fgene.2025.1722189

Received: 10 October 2025; Accepted: 21 October 2025;
Published: 07 November 2025.

Approved by:

Frontiers Editorial Office, Frontiers Media SA, Switzerland

Copyright © 2025 Hu, Liang, Liu, Jiang, Xie, Zhou and Zhang. 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: Xin Zhou, MTg4NjYxMTUyNTFAMTYzLmNvbQ==; Xiaojia Zhang, enhqMTk4ODA2MjVAMTYzLmNvbQ==

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.