作者：
Meret,Wegler [1]
;
Xiangbin,Jia [2]
;
Marielle,Alders [3]
;
Arjan,Bouman [4]
;
Jia,Chen [2]
;
Xinyu,Duan [5]
;
Julie L,Lauzon [6]
;
Inge B,Mathijssen [3]
;
Heinrich,Sticht [7]
;
Steffen,Syrbe [8]
;
Senwei,Tan [2]
;
Hui,Guo [9]
;
Rami,Abou Jamra [10]
作者单位：
Institute of Human Genetics, University Medical Center, Leipzig, Germany.
[1]
Center for Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
[2]
Department of Human Genetics, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
[3]
Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, The Netherlands.
[4]
Department of Pediatrics, Daping Hospital, Army Medical University, Chongqing, China.
[5]
Department of Medical Genetics, Cummings School of Medicine, University of Calgary, Alberta Children's Hospital, Alberta, Canada.
[6]
Institute of Biochemistry, Medical Faculty, Friedrich-Alexander-Universität Erlangen-Nürnberg; Erlangen, Germany.
[7]
Division of Pediatric Epileptology, Centre for Pediatrics and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany.
[8]
Center for Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China. Electronic address: guohui2@csu.edu.cn.
[9]
Institute of Human Genetics, University Medical Center, Leipzig, Germany. Electronic address: rami.aboujamra@medizin.uni-leipzig.de.
[10]
DOI
10.1016/j.gim.2022.04.013
PMID
35511136
发布时间
2022-12-07
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