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CORRECTION article

Front. Genet., 21 October 2022
Sec. Genetics of Common and Rare Diseases
Volume 13 - 2022 | https://doi.org/10.3389/fgene.2022.1036144

Corrigendum: Identification of the first congenital ichthyosis case caused by a homozygous deletion in the ALOX12B gene due to chromosome 17 mixed uniparental disomy

This article is a correction to:

  1. Identification of the first congenital ichthyosis case caused by a homozygous deletion in the ALOX12B gene due to chromosome 17 mixed uniparental disomy

    1. Read original article
Lei Zhang&#x;Lei Zhang1†Yanqiu Hu&#x;Yanqiu Hu1†Jingjing Lu&#x;Jingjing Lu2†Peiwei ZhaoPeiwei Zhao1Xiankai ZhangXiankai Zhang1Li TanLi Tan1Jun LiJun Li3Cuiping Xiao Cuiping Xiao1*Linkong Zeng Linkong Zeng4*Xuelian He Xuelian He1*
  • 1Precision Medical Center, Wuhan Children’s Hospital (Wuhan Maternal and Child Healthcare Hospital), Tongji Medical College, Huazhong University of Science & Technology, Wuhan, China
  • 2Dermatology Department, Wuhan Children’s Hospital (Wuhan Maternal and Child Healthcare Hospital), Tongji Medical College, Huazhong University of Science & Technology, Wuhan, China
  • 3Otolaryngology Department, Wuhan Children’s Hospital (Wuhan Maternal and Child Healthcare Hospital), Tongji Medical College, Huazhong University of Science & Technology, Wuhan, China
  • 4Neonatology Department, Wuhan Children’s Hospital (Wuhan Maternal and Child Healthcare Hospital), Tongji Medical College, Huazhong University of Science & Technology, Wuhan, China

A Corrigendum on
Identification of the first congenital ichthyosis case caused by a homozygous deletion in the ALOX12B gene due to chromosome 17 mixed uniparental disomy

by Zhang L, Hu Y, Lu J, Zhao P, Zhang X, Tan L, Li J, Xiao C, Zeng L and He X (2022). Front. Genet. 13:931833. doi: 10.3389/fgene.2022.931833

In the published article, there was an error in affiliations 1, 2, and 3.

In all three affiliations, “Huazhong University of Science & Technology, Wuhan, China”, should be “Wuhan Children’s Hospital (Wuhan Maternal and Child Healthcare), Tongji Medical College, Huazhong University of Science & Technology, Wuhan, China”.

The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.

Keywords: ARCI, ALOX12B, whole-exome sequencing, mixed UPD (mixUPD), microtia

Citation: Zhang L, Hu Y, Lu J, Zhao P, Zhang X, Tan L, Li J, Xiao C, Zeng L and He X (2022) Corrigendum: Identification of the first congenital ichthyosis case caused by a homozygous deletion in the ALOX12B gene due to chromosome 17 mixed uniparental disomy. Front. Genet. 13:1036144. doi: 10.3389/fgene.2022.1036144

Received: 04 September 2022; Accepted: 28 September 2022;
Published: 21 October 2022.

Edited and reviewed by:

Lidia Larizza, Research Lab of Medical Cytogenetics and Molecular Genetics, Italian Auxological Institute (IRCCS), Italy

Copyright © 2022 Zhang, Hu, Lu, Zhao, Zhang, Tan, Li, Xiao, Zeng and He. 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: Xuelian He, aGV4dWVsaWFuMjAxM0Bob3RtYWlsLmNvbQ==; Cuiping Xiao, NDU5NTE4MjQwQHFxLmNvbQ==; Linkong Zeng, ZnJlZW1hbjMxNUAxNjMuY29t

†These authors have contributed equally to this work

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.