CORRECTION article

Front. Genet., 15 August 2023

Sec. Genetics of Common and Rare Diseases

Volume 14 - 2023 | https://doi.org/10.3389/fgene.2023.1273023

Corrigendum: A heterozygous mutation in NOTCH3 in a Chinese family with CADASIL

  • 1. Department of Pharmacy, The Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China

  • 2. Department of Neurology, The Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China

  • 3. Department of Pain, The Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China

  • 4. Department of Endocrinology, The Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China

  • 5. Department of Pharmacy, Taihe Hospital, Hubei University of Medicine, Shiyan, Hubei, China

  • 6. Department of Prenatal Diagnostic Center, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangdong, China

  • 7. School of Pharmacy, Hubei University of Science and Technology, Xianning, China

  • 8. Department of Pediatrics, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, Hubei, China

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In the published article, there was an error in the Funding statement. “A fund (Central Guiding Local Science and Technology Development Special Project, No. 2022BGE272) which supports our work was not included in the article.” The correct Funding statement appears below.

“This study was supported by the Health and Family Planning Commission of Wuhan City (WX18M02) and Central Guiding Local Science and Technology Development Special Project (No. 2022BGE272).”

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.

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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.

Summary

Keywords

CADASIL, whole-exome-sequencing, heterozygous, Notch3, treatment scheme

Citation

Li J, Luo T, Wang X, Wang M, Zheng T, Dang X, Deng A, Zhang Y, Ding S, Jing P and Zhu L (2023) Corrigendum: A heterozygous mutation in NOTCH3 in a Chinese family with CADASIL. Front. Genet. 14:1273023. doi: 10.3389/fgene.2023.1273023

Received

05 August 2023

Accepted

07 August 2023

Published

15 August 2023

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Frontiers Editorial Office, Frontiers Media SA, Switzerland

Volume

14 - 2023

Updates

Copyright

*Correspondence: Sheng Ding, ; Ping Jing, ; Lin Zhu,

†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.

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