作者：
Nan,Pang [1]
;
Kuokuo,Li [2]
;
Senwei,Tan [3]
;
Meilin,Chen [3]
;
Fang,He [1]
;
Chen,Chen [1]
;
Lifen,Yang [1]
;
Ciliu,Zhang [1]
;
Xiaolu,Deng [1]
;
Li,Yang [1]
;
Leilei,Mao [1]
;
Guoli,Wang [1]
;
Haolin,Duan [1]
;
Xiaole,Wang [1]
;
Wen,Zhang [1]
;
Hui,Guo [3]
;
Jing,Peng [4]
;
Fei,Yin [5]
;
Kun,Xia [6]
作者单位：
Department of Pediatrics, Xiangya Hospital, Central South University, Changsha 410008, China; Clinical Research Center for Children Neurodevelopmental Disabilities of Hunan Province, Xiangya Hospital, Central South University, Changsha 410008, China.
[1]
Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan 410078, China; Department of Obstetrics and Gynecology, The First Affiliated Hospital of Anhui Medical University, Hefei 230022, China.
[2]
Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan 410078, China.
[3]
Department of Pediatrics, Xiangya Hospital, Central South University, Changsha 410008, China; Clinical Research Center for Children Neurodevelopmental Disabilities of Hunan Province, Xiangya Hospital, Central South University, Changsha 410008, China. Electronic address: pengjing4346@163.com.
[4]
Department of Pediatrics, Xiangya Hospital, Central South University, Changsha 410008, China; Clinical Research Center for Children Neurodevelopmental Disabilities of Hunan Province, Xiangya Hospital, Central South University, Changsha 410008, China. Electronic address: yf2323@hotmail.com.
[5]
Center for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan 410078, China; Hengyang Medical School, 421001, University of South, China. Electronic address: xiakun@sklmg.edu.cn.
[6]
DOI
10.1016/j.gene.2023.148071
PMID
38081334
发布时间
2024-01-17
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