De Kovel, Carolien G. F. Language and Genetics Department, MPI for Psycholinguistics, Max Planck Society; Department of Genetics, University Medical Center Utrecht;
DeKovel_etal_2017a.pdf (Publisher version), 2MB
De Kovel, C. G. F., Syrbe, S., Brilstra, E. H., Verbeek, N., Kerr, B., Dubbs, H., et al. (2017). Neurodevelopmental Disorders Caused by De Novo Variants in KCNB1 Genotypes and Phenotypes. JAMA Neurology, 74(10), 1228-1236. doi:10.1001/jamaneurol.2017.1714.