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.
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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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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