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

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

Affiliations

Jinying Wu

Tianjin Pediatric Research Institute, Tianjin Children’s Hospital (Children’s Hospital of Tianjin University)

Meifang Lei

Department of Neurology, Tianjin Children’s Hospital (Children’s Hospital of Tianjin University)

Xuetao Wang

Tianjin Pediatric Research Institute, Tianjin Children’s Hospital (Children’s Hospital of Tianjin University)

Nan Liu

Tianjin Pediatric Research Institute, Tianjin Children’s Hospital (Children’s Hospital of Tianjin University)

Xiaowei Xu

Tianjin Pediatric Research Institute, Tianjin Children’s Hospital (Children’s Hospital of Tianjin University)

Chunyu Gu

Tianjin Pediatric Research Institute, Tianjin Children’s Hospital (Children’s Hospital of Tianjin University)

Yuping Yu

Graduate College of Tianjin Medical University

Wei Liu

Tianjin Children’s Hospital (Children’s Hospital of Tianjin University)