Kortüm, Fanny
Jamra, Rami Abou http://orcid.org/0000-0002-1542-1399
Alawi, Malik
Berry, Susan A.
Borck, Guntram http://orcid.org/0000-0003-2279-8052
Helbig, Katherine L.
Tang, Sha
Huhle, Dagmar
Korenke, Georg Christoph
Hebbar, Malavika
Shukla, Anju
Girisha, Katta M.
Steinlin, Maja
Waldmeier-Wilhelm, Sandra
Montomoli, Martino
Guerrini, Renzo
Lemke, Johannes R.
Kutsche, Kerstin
Article History
Received: 21 August 2017
Revised: 28 December 2017
Accepted: 9 January 2018
First Online: 20 February 2018
Compliance with Ethical Standards
:
: K.L.H. was and S.T. is employed by and receive a salary from Ambry Genetics; whole-exome sequencing is among its commercially available tests. D.H. is employed by and receives a salary from MVZ Labor Leipzig. R.G. has received travel funding and honoraria for Advisory Board activities from Eisai, Inc., Novartis, and Zogenix; has received travel funding from UCB; has served on the editorial boards of Epilepsia, Progress in Epileptic Disorders, Neuropediatrics, the Journal of Child Neurology, Seizure, BMC Medical Genetics, Topics in Epilepsy, the Journal of Pediatric Epilepsy, Epileptic Disorders, the European Neurological Journal, Neurology, and the Journal of Embryology and Developmental Biology; receives publishing royalties from Cambridge University Press, Lippincott Williams and Wilkins, John Libbey Eurotext, and Oxford University Press; and has received research support from the European Union, Tuscany Region Research Department, EC, Italian Ministry of Health and, and the Pisa Foundation. The other authors report no disclosures relevant to the manuscript.