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作者：
Maria B. Christensen [1]
;
Amanda M. Levy [2]
;
Nazanin A. Mohammadi [3]
;
Marcello Niceta [4]
;
Rauan Kaiyrzhanov [5]
;
Maria Lisa Dentici [6]
;
Chadi Al Alam [7]
;
Viola Alesi [8]
;
Valérie Benoit [9]
;
Kailash P. Bhatia [10]
;
Tatjana Bierhals [11]
;
Christian M. Bo?elmann [12]
;
Julien Buratti [13]
;
Bert Callewaert [14]
;
Berten Ceulemans [15]
;
Perrine Charles [16]
;
Matthias De Wachter [17]
;
Mohammadreza Dehghani [18]
;
Erika D'haenens [19]
;
Martine Doco‐Fenzy [20]
;
Michaela Ge?ner [21]
;
Cyrielle Gobert [22]
;
Ulviyya Guliyeva [23]
;
Tobias B. Haack [24]
;
Trine B. Hammer [25]
;
Tilman Heinrich [26]
;
Maja Hempel [27]
;
Theresia Herget [28]
;
Ute Hoffmann [29]
;
Judit Horvath [30]
;
Henry Houlden [31]
;
Boris Keren [32]
;
Christina Kresge [33]
;
Candy Kumps ;
Damien Lederer ;
Alban Lermine ;
Francesca Magrinelli ;
Reza Maroofian ;
Mohammad Yahya Vahidi Mehrjardi ;
Mahdiyeh Moudi ;
Amelie J. Müller ;
Anna J. Oostra ;
Beth A. Pletcher ;
David Ros‐Pardo ;
Shanika Samarasekera ;
Marco Tartaglia ;
Kristof Van Schil ;
Julie Vogt ;
Evangeline Wassmer ;
Juliane Winkelmann ;
Maha S. Zaki ;
Michael Zech ;
Holger Lerche ;
Francesca Clementina Radio ;
Paulino Gomez‐Puertas ;
Rikke S. M?ller ;
Zeynep Tümer
作者单位：
Department of Clinical Genetics,Copenhagen University Hospital
[1]
Kennedy Center, Department of Clinical Genetics,Copenhagen University Hospital
[2]
Department of Epilepsy Genetics and Personalized Treatment,The Danish Epilepsy Centre
[3]
Genetics and Rare Diseases Research Division,Ospedale Pediatrico Bambino Gesù, IRCCS
[4]
Department of Neuromuscular Disorders,University College London Institute of Neurology
[5]
Pediatric Neurology department,American center for Psychiatry and Neurology
[6]
Translational Cytogenomics Research Unit,Ospedale Pediatrico Bambino Gesù, IRCCS
[7]
IPG,Centre for Human Genetics
[8]
Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology
[9]
Institute of Human Genetics,University Medical Center Hamburg‐Eppendorf
[10]
Department of Neurology and Epileptology, Hertie‐Institute for Clinical Brain Research,University
[11]
Department of Medical Genetics, Pitié‐Salpêtrière Hospital,AP‐HP, Sorbonne Université
[12]
Center for Medical Genetics,Ghent University Hospital
[13]
Department of Pediatric Neurology, Antwerp University Hospital,University of Antwerp
[14]
Medical Genetics Research Center,Shahid Sadoughi University of Medical Sciences
[15]
SFR CAP SANTE,HMB2 CHU Reims
[16]
KfH‐Board of Trustees for Dialysis and Kidney Transplantation (KfH‐Kuratorium für Dialyse und
[17]
Neuropediatric department,Centre Hospitalier Neurologique William Lennox
[18]
Department of Pediatrics,MediClub Hospital
[19]
Institute of Medical Genetics and Applied Genomics,University of Tübingen
[20]
St. Franziskus‐Hospital
[21]
Institute of Human Genetics,University of Münster
[22]
Department of Pediatrics,Rutgers New Jersey Medical School
[23]
LBBMS SeqOIA,AP‐HP
[24]
Department of Genetics,Shahid Sadoughi University of Medical Sciences
[25]
Neuropediatric department,Ghent University Hospital
[26]
Molecular Modeling Group,Centro de Biología Molecular Severo Ochoa, CBMSO (CSIC‐UAM)
[27]
Neurology Department,Queen Elizabeth Hospital
[28]
Department of Medical Genetics, Antwerp University Hospital,University of Antwerp
[29]
West Midlands Regional Genetics Service,Birmingham Women's and Children's Hospital
[30]
Neurology Department,Birmingham Women and Children's Hospital
[31]
Institute of Human Genetics, School of Medicine,Technical University of Munich
[32]
Clinical Genetics Department, Human Genetics and Genome Research Institute,National Research Centre
[33]
发布时间
2022-10-05
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