Shi, Xinmiao
Shi, Ying
Zhang, Luxia
Gan, Lanxia
Zhong, Xuhui
Huang, Yuming
Yao, Chen
Wang, Yanfang
Dong, Chongya
Liu, Beini
Wang, Fang
Wang, Haibo
Ding, Jie
Funding for this research was provided by:
the National Key Research and Development Program of China, the registry study of rare diseases in children (2016YFC0901505)
Beijing Key laboratory of molecular diagnosis and study on pediatric genetic diseases (BZ0317)
Article History
Received: 12 October 2020
Accepted: 13 April 2021
First Online: 25 May 2021
Declarations
:
: This study was approved by Peking University First Hospital Institutional Review Board (2017(19)). Informed consent was obtained from a parent and/or legal guardians of subjects. All methods were carried out in accordance with relevant guidelines and regulations.
: Not applicable.
: The authors declare that they have no competing interests.