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Correction: Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report

Italian Journal of Pediatrics volume 49, Article number: 32 (2023) Cite this article

The Original Article was published on 29 December 2022

Correction: Ital J Pediatr 48, 204 (2022)

https://doi.org/10.1186/s13052-022-01398-0

The original article [1] mistakenly mis-numbered a section of citations in the main body; this has since been rectified.

Reference

  1. Jinying W, et al. Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report. Ital J Pediatr. 2022;48:204. https://doi.org/10.1186/s13052-022-01398-0.

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Authors and Affiliations

  1. Tianjin Pediatric Research Institute, Tianjin Children’s Hospital (Children’s Hospital of Tianjin University), Tianjin, 300134, China

    Jinying Wu, Xuetao Wang, Nan Liu, Xiaowei Xu & Chunyu Gu

  2. Tianjin Key Laboratory of Birth Defects for Prevention and Treatment, Tianjin, 300134, China

    Jinying Wu, Xuetao Wang, Nan Liu, Xiaowei Xu & Chunyu Gu

  3. Department of Neurology, Tianjin Children’s Hospital (Children’s Hospital of Tianjin University), Tianjin, 300134, China

    Meifang Lei

  4. Graduate College of Tianjin Medical University, Tianjin, 300070, China

    Yuping Yu

  5. Tianjin Children’s Hospital (Children’s Hospital of Tianjin University), Tianjin, 300134, China

    Wei Liu

Authors
  1. Jinying Wu
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  2. Meifang Lei
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  3. Xuetao Wang
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  4. Nan Liu
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  5. Xiaowei Xu
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  6. Chunyu Gu
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  7. Yuping Yu
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  8. Wei Liu
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Corresponding author

Correspondence to Wei Liu.

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Wu, J., Lei, M., Wang, X. et al. Correction: Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report. Ital J Pediatr 49, 32 (2023). https://doi.org/10.1186/s13052-023-01433-8

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  • DOI: https://doi.org/10.1186/s13052-023-01433-8

Italian Journal of Pediatrics

ISSN: 1824-7288

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