Luo, Jiaxin
Liu, Peisen
chen, Pengxi
Zhou, Xia
Ma, Yueru
Lin, Wenxiao
Lai, Keying
Cui, Jingyi
Mi, Chunmei
Wu, Xi
Yuan, Xiying
Ke, Weilin
Li, Zhuo
Wu, Lingqian
Funding for this research was provided by:
the Hunan Provincial Natural Science Foundation of China (2023JJ30725)
the Open Research fund of Hunan Provincial Key Laboratory of Regional Hereditary Birth Defects Prevention and Control (HPKL2023004)
the Open Research Fund of Hainan Province Clinical Medical Center (HNSZLAB202403)
National Key Research and Development Program of China (2022YFC2703700)
National Key Research and Development Program of China (2022YFC2703700)
Innovative Research Group Project of the National Natural Science Foundation of China (82171711)
Article History
Received: 14 November 2025
Accepted: 9 February 2026
First Online: 20 February 2026
Declarations
:
: The authors declare no competing interests.
: The studies involving humans were approved by Ethics Committee of the Center for Medical Genetics, Central South University, Hunan, China (approval no.: 2021-1-26). The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study.