Published in:

Open Access 01-12-2023 | Correction

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

Authors: Jinying Wu, Meifang Lei, Xuetao Wang, Nan Liu, Xiaowei Xu, Chunyu Gu, Yuping Yu, Wei Liu

Published in: Italian Journal of Pediatrics | Issue 1/2023