作者：
Maljevic, Snezana [1]
;
Keren, Boris [2]
;
Aung, Ye Htet [3]
;
Forster, Ian C. [4]
;
Mignot, Cyril [5]
;
Buratti, Julien [6]
;
Lafitte, Aurelie [7]
;
Freihuber, Cecile [8]
;
Rodan, Lance H. [9]
;
Bergin, Ann [10]
;
Hubert, Laurence ;
Poirier, Karine ;
Munnich, Arnold ;
Besmond, Claude ;
Hauser, Natalie ;
Miller, Rebecca ;
McWalter, Kirsty ;
Nabbout, Rima ;
Heron, Delphine ;
Leguern, Eric ;
Depienne, Christel ;
Petrou, Steven ;
Nava, Caroline
作者单位：
Hop Necker Enfants Malad, AP HP, Ctr Reference Epilesies Rares, Serv Neurol Pediat, Paris, France
[1]
Harvard Med Sch, Boston Childrens Hosp, Div Genet & Genom, Boston, MA 02115 USA
[2]
Paris Descartes Univ, Translat Genet Lab, Imagine Inst, INSERM,UMR 1163, Paris, France
[3]
GeneDx, Gaithersburg, MD USA
[4]
Sorbonne Univ, Inst Cerveau & Moelle Epiniere, ICM, INSERM,U1127,CNRS,UMR 7225, F-75013 Paris
[5]
Inova Translat Med Inst, Inova Hlth Syst, Falls Church, VA USA
[6]
Hop La Pitie Salpetriere, AP HP, Ctr Reference Deficience Intellectuelle Causes Ra, GRC UPMC
[7]
Harvard Med Sch, Boston Childrens Hosp, Dept Neurol, Div Epilepsy & Clin Neurophysiol, Boston, MA
[8]
Hop Trousseau, AP HP, Serv Neuropediat, Paris, France
[9]
Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Melbourne, Vic, Australia
[10]
发布时间
2019-11-26
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