CORRECTION article

Front. Pediatr., 21 November 2022

Sec. Genetics of Common and Rare Diseases

Volume 10 - 2022 | https://doi.org/10.3389/fped.2022.1074856

Corrigendum: Dietary fiber and probiotics based on gut microbiota targeting for functional constipation in children with cerebral palsy

  • 1. Department of Pediatrics, Longgang District Maternity and Child Healthcare Hospital, Shenzhen, China

  • 2. Department of Obstetrics and Gynecology, Peking University Shenzhen Hospital, Shenzhen, China

  • 3. Shenzhen Middle School, Shenzhen, China

  • 4. Department of Nutrition, BGI Nutrition Precision Co., Ltd., Shenzhen, China

  • 5. The Outpatient Department, Longgang District Social Welfare Center, Shenzhen, China

  • 6. Department of Microbial Research, WeHealthGene Institute, Joint Laboratory of Micro-Ecology and Children’s Health, Shenzhen Children’s Hospital, Shenzhen WeHealthGene Co., Ltd., Shenzhen, China

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In the published article, author Chunuo Chu was omitted from co-first authorship. The corrected author list appears below.

Congfu Huang1†, Jinli Lyu2†, Chunuo Chu3†, Lan Ge4, Yuanping Peng5, Zhenyu Yang6, Shenghua Xiong1, Bin Wu1, Xiao Chen1 and Xiaowei Zhang2*.

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

gut microbiota, dietary fiber, probiotics, cerebral palsy, functional constipation

Citation

Huang C, Lyu J, Chu C, Ge L, Peng Y, Yang Z, Xiong S, Wu B, Chen X and Zhang X (2022) Corrigendum: Dietary fiber and probiotics based on gut microbiota targeting for functional constipation in children with cerebral palsy. Front. Pediatr. 10:1074856. doi: 10.3389/fped.2022.1074856

Received

20 October 2022

Accepted

21 October 2022

Published

21 November 2022

Approved by

Frontiers in Pediatrics, Frontiers Media SA, Switzerland

Volume

10 - 2022

Updates

Copyright

*Correspondence: Xiaowei Zhang

These authors have contributed equally to this work and share first authorship

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

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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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