作者：
Novara, Francesca [1]
;
Rinaldi, Berardo [2]
;
Sisodiya, Sanjay M. [3]
;
Coppola, Antonietta [4]
;
Giglio, Sabrina [5]
;
Stanzial, Franco [6]
;
Benedicenti, Francesco [7]
;
Donaldson, Alan [8]
;
Andrieux, Joris [9]
;
Stapleton, Rachel [10]
;
Weber, Astrid [11]
;
Reho, Paolo [12]
;
van Ravenswaaij-Arts, Conny [13]
;
Kerstjens-Frederikse, Wilhelmina S. [14]
;
Vermeesch, Joris Robert [15]
;
Devriendt, Koenraad ;
Bacino, Carlos A. ;
Delahaye, Andree ;
Maas, S. M. ;
Iolascon, Achille ;
Zuffardi, Orsetta
作者单位：
St Michaels Hosp, Dept Clin Genet, Bristol, Avon, England
[1]
Acad Med Ctr, Dept Pediat, Amsterdam, Netherlands
[2]
Azienda Sanit Alto Adige, Ctr Prov Coordinamento Rete Malattie Rare, Serv Consulenza Genet, Bolzano
[3]
Robert Debre Univ Hosp, INSERM, UMR 1141, Paris, France
[4]
NIHR Univ Coll London Hosp Biomed Res Ctr, UCL Inst Neurol, Dept Clin & Expt Epilepsy, London
[5]
Univ Napoli Federico II, Dipartimento Med Mol & Biotecnol Med, Naples, Italy
[6]
Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[7]
Univ Naples Federico II, Dept Neurosci Reprod & Odontostomatol Sci, Epilepsy Ctr, Naples, Italy
[8]
Univ Groningen, Univ Med Ctr Groningen, Dept Genet, Groningen, Netherlands
[9]
Univ Pavia, Dept Mol Med, Via Forlanini 14, I-27100 Pavia, Italy
[10]
Auckland City Hosp, Genet Hlth Serv NZ Northern Hub, Bldg 30, Auckland, New Zealand
[11]
Univ Florence, Dept Clin & Expt Biomed Sci Mario Serio, Med Genet Unit, Florence, Italy
[12]
CHRU Lille, Hop Jeanne de Flandre, Inst Genet Med, Lille, France
[13]
Katholieke Univ Leuven, Ctr Human Genet, Lab Cytogenet & Genome Res, Leuven, Belgium
[14]
Liverpool Womens NHS Fdn Hosp Trust, Merseyside & Cheshire Clin Genet Serv, Liverpool, Merseyside
[15]
发布时间
2018-06-23
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