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

  • 1. Precision Medical Center, Wuhan Children’s Hospital (Wuhan Maternal and Child Healthcare Hospital), Tongji Medical College, Huazhong University of Science & Technology, Wuhan, China

  • 2. Dermatology Department, Wuhan Children’s Hospital (Wuhan Maternal and Child Healthcare Hospital), Tongji Medical College, Huazhong University of Science & Technology, Wuhan, China

  • 3. Otolaryngology Department, Wuhan Children’s Hospital (Wuhan Maternal and Child Healthcare Hospital), Tongji Medical College, Huazhong University of Science & Technology, Wuhan, China

  • 4. Neonatology Department, Wuhan Children’s Hospital (Wuhan Maternal and Child Healthcare Hospital), Tongji Medical College, Huazhong University of Science & Technology, Wuhan, China

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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.

Summary

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

Volume

13 - 2022

Edited and reviewed by

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

Updates

Copyright

*Correspondence: Xuelian He, ; Cuiping Xiao, ; Linkong Zeng,

†These authors have contributed equally to this work

This article was submitted to Genetics of Common and Rare Diseases, a section of the journal Frontiers in Genetics

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.

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