@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",
}