Front. Genet.Frontiers in GeneticsFront. Genet.1664-8021Frontiers Media S.A.127302310.3389/fgene.2023.1273023GeneticsCorrectionCorrigendum: A heterozygous mutation in NOTCH3 in a Chinese family with CADASILLi et al.10.3389/fgene.2023.1273023LiJuyi1†LuoTao2†WangXiufang3†WangMengjie4†ZhengTao5DangXiao6DengAiping1ZhangYouzhi7DingSheng4*JingPing2*ZhuLin8*1Department of Pharmacy, The Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China2Department of Neurology, The Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China3Department of Pain, The Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China4Department of Endocrinology, The Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China5Department of Pharmacy, Taihe Hospital, Hubei University of Medicine, Shiyan, Hubei, China6Department of Prenatal Diagnostic Center, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangdong, China7School of Pharmacy, Hubei University of Science and Technology, Xianning, China8Department of Pediatrics, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, Hubei, China
Approved by:Frontiers Editorial Office, Frontiers Media SA, Switzerland
*Correspondence: Sheng Ding, doctordingsheng@163.com; Ping Jing, jing51118@sina.com; Lin Zhu, zhulinhust@hust.edu.cn
These authors have contributed equally to this work
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.
A Corrigendum on A heterozygous mutation in NOTCH3 in a Chinese family with CADASIL by Li J, Luo T, Wang X, Wang M, Zheng T, Dang X, Deng A, Zhang Y, Ding S, Jing P and Zhu L (2022). Front. Genet. 13:943117. doi: 10.3389/fgene.2022.943117CADASILwhole-exome-sequencingheterozygousNotch3treatment schemesection-at-acceptanceGenetics of Common and Rare Diseases
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.
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.