CORRECTION article
Front. Genet.
Sec. Genetics of Common and Rare Diseases
Correction: Identification of a novel ANK1 gene variant c.1504-9G>A and its mechanism of intron retention in hereditary spherocytosis
Provisionally accepted
- Jiangxi Provincial Children's Hospital, Nanchang, China
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Correction on: Xiong T, Xu Z, Wan Q, Chen F, Ye Y, Wang H and Wu C (2024) Identification of a novel ANK1 gene variant c.1504-9G>A and its mechanism of intron retention in hereditary spherocytosis. Front. Genet. 15:1390924. doi: 10.3389/fgene.2024.1390924 Adding/removing text In the originally published article, the ANK1 gene variant was incorrectly reported using transcript NM_020475.2 in the section of 2.2.3 Pathogenic variant confirmation. The correct reference transcript should be NM_001142446. The original version of this article has been updated.
Keywords: ANK1, Hereditary spherocytosis, Intron retention, minigene splicing assay, Whole-exome sequencing
Received: 07 Dec 2025; Accepted: 12 Dec 2025.
Copyright: © 2025 Xiong, Xu, Wan, Chen, Ye, Wang and Wu. 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: Chongjun Wu
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