@article{87cddad2665e406699db3f4a10c4bd55,
title = "Rare gene deletions in genetic generalized and Rolandic epilepsies",
keywords = "GENOME-WIDE ASSOCIATION, AUTISM CANDIDATE GENES, COPY NUMBER VARIATION, DE-NOVO MUTATIONS, STRUCTURAL VARIATION, DEVELOPMENTAL DELAY, PARKINSONS-DISEASE, RISK LOCI, VARIANTS, DISORDERS, 3111 Biomedicine, 3112 Neurosciences, 3124 Neurology and psychiatry",
author = "\{EuroEPINOMICS-CoGIE Consortium\} and Kamel Jabbari and Bobbili, \{Dheeraj R.\} and Dennis Lal and Reinthaler, \{Eva M.\} and Julian Schubert and Stefan Wolking and Vishal Sinha and Susanne Motameny and Holger Thiele and Amit Kawalia and Janine Altmueller and Toliat, \{Mohammad Reza\} and Robert Kraaij and \{van Rooij\}, Jeroen and Uitterlinden, \{Andre G.\} and Ikram, \{M. Arfan\} and Federico Zara and Anna-Elina Lehesjoki and Roland Krause and Fritz Zimprich and Thomas Sander and Neubauer, \{Bernd A.\} and Patrick May and Holger Lerche and Peter Nuernberg",
year = "2018",
month = aug,
day = "27",
doi = "10.1371/journal.pone.0202022",
language = "English",
volume = "13",
journal = "PLoS One",
issn = "1932-6203",
publisher = "Public Library of Science",
number = "8",
}