作者：
Heinzen,E.L. [1]
;
Arzimanoglou,A. [2]
;
Brashear,A. [3]
;
Clapcote,S.J. [4]
;
Gurrieri,F. [5]
;
Goldstein,D.B. [6]
;
Jóhannesson,S.H. [7]
;
Mikati,M.A. [8]
;
Neville,B. [9]
;
Nicole,S. [10]
;
Ozelius,L.J. [11]
;
Poulsen,H. [12]
;
Schyns,T. [13]
;
Sweadner,K.J. [14]
;
vandenMaagdenberg,A. [15]
;
Vilsen,B.
作者单位：
Istituto di Genetica Medica, Università Cattolica S Cuore, Rome, Italy
[1]
Division of Pediatric Neurology, Duke University, School of Medicine, Durham, NC, United States
[2]
Institute of Child Health, University College London, London, United Kingdom
[3]
Center for Human Genome Variation, Duke University, School of Medicine, Durham, NC, United States
[4]
Department of Human Genetics and Department of Neurology, Leiden University Medical Centre, Leiden
[5]
Danish Research Institute for Translational Neuroscience, Nordic-EMBL Partnership of Molecular
[6]
Department of Genetics and Genomic Sciences and Department of Neurology, Icahn School of Medicine
[7]
Neurosurgery, Massachusetts General Hospital, Boston, MA, United States
[8]
AHC Federation of Europe and AHC Association of Iceland, Reykjavik, Iceland
[9]
Department of Biomedicine, Aarhus University, Aarhus, Denmark
[10]
Epilepsy, Sleep and Pediatric Neurophysiology Department, HFME, University Hospitals of Lyon
[11]
Department of Neurology, Wake Forest School of Medicine, Winston Salem, NC, United States
[12]
European Network for Research on Alternating Hemiplegia (ENRAH), Brussels, Belgium
[13]
School of Biomedical Sciences, University of Leeds, Leeds, United Kingdom
[14]
Institut National de la Santé et de la Recherche Médicale, U975, Centre de Recherche de l'Institut
[15]
发布时间
2014-06-29
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