作者:
Amélie,Cordovado [1]
;
Martina,Schaettin [2]
;
Médéric,Jeanne [3]
;
Veranika,Panasenkava [4]
;
Anne-Sophie,Denommé-Pichon [5]
;
Boris,Keren [6]
;
Cyril,Mignot [7]
;
Martine,Doco-Fenzy [8]
;
Lance,Rodan [9]
;
Keri,Ramsey [10]
;
Vinodh,Narayanan [11]
;
Julie R,Jones [12]
;
Eloise J,Prijoles [13]
;
Wendy G,Mitchell [14]
;
Jillian R,Ozmore [15]
;
Kali,Juliette [16]
;
Erin,Torti [17]
;
Elizabeth A,Normand [18]
;
Leslie,Granger [19]
;
Andrea K,Petersen [20]
;
Margaret G,Au [21]
;
Juliann P,Matheny [22]
;
Chanika,Phornphutkul [23]
;
Mary-Kathryn,Chambers [24]
;
Joaquín-Alejandro,Fernández-Ramos [25]
;
Eduardo,López-Laso [26]
;
Michael C,Kruer [27]
;
Somayeh,Bakhtiari [28]
;
Marcella,Zollino ;
Manuela,Morleo ;
Giuseppe,Marangi ;
Davide,Mei ;
Tiziana,Pisano ;
Renzo,Guerrini ;
Raymond J,Louie ;
Anna,Childers ;
David B,Everman ;
Betrand,Isidor ;
Séverine,Audebert-Bellanger ;
Sylvie,Odent ;
Dominique,Bonneau ;
Brigitte,Gilbert-Dussardier ;
Richard,Redon ;
Stéphane,Bézieau ;
Frédéric,Laumonnier ;
Esther T,Stoeckli ;
Annick,Toutain ;
Marie-Laure,Vuillaume
作者单位:
UMR 1253, iBrain, University of Tours, INSERM
[1]
Department of Molecular Life Sciences
[2]
Functional Unit in Innovative Genomic Diagnosis of Rare Diseases, FHU-TRANSLAD, Dijon-Bourgogne
[3]
Genetics Department, Pitié-Salpêtrière Hospital, AP-HP. Sorbonne University
[4]
University Hospital Reims, AMH2, Genetics Division, SFR CAP santé EA3801
[5]
Division of Genetics and Genomics
[6]
Center for Rare Childhood Disorders, Translational Genomics Research Institute
[7]
Molecular Diagnostic Laboratory, Greenwood Genetic Center
[8]
Greenwood Genetic Center
[9]
Neurology Division
[10]
Dartmouth Hitchcock Medical Center
[11]
Neurology Department, Gillette Children's Specialty Healthcare
[12]
GeneDx
[13]
Genetics Division
[14]
Department of Genetics and Metabolism, University of Kentucky
[15]
Division of Human Genetics
[16]
Division of Genetics, Rhode Island Hospital, Hasbro Children's Hospital
[17]
Pediatric Neurology Unit
[18]
Pediatric Movement Disorders Program
[19]
Università Cattolica Sacro Cuore, Dipartimento Scienze della Vita e Sanità Pubblica, Sezione di
[20]
Telethon Institute of Genetics and Medicine (TIGEM)
[21]
Pediatric Neurology
[22]
Medical Genetics Service
[23]
Clinical Genetics Service, University Hospital of Brest, Morvan Hospital
[24]
Clinical Genetics Service, University Hospital, Genetic and Development Institute of Rennes IGDR
[25]
Department of Medical Genetics, University Hospital of Angers and Mitovasc INSERM 1083
[26]
Medical Genetics, University Hospital, La Milétrie, BP 577
[27]
INSERM, CNRS, UNIV Nantes, Thorax Institute
[28]
发布时间
2023-02-04
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Human Molecular Genetics
Human Molecular Genetics
3325-3340页
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