Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects - Niestroj, Lisa-Marie; Perez-Palma, Eduardo; Howrigan, Daniel P; Zhou, Yadi; Cheng, Feixiong; Saarentaus, Elmo; Nürnberg, Peter; Stevelink, Remi; Daly, Mark J; Palotie, Aarno; Lal, Dennis; Feng, Yen-Chen Anne; et al. (Brain (London, England : 1878), 2020)
Keywords: DNA Copy Number Variations - genetics; Epilepsy - genetics; Female; Genetic Predisposition to Disease - genetics; Genome-Wide Association Study; Humans; Male; Original; epilepsy; developmental and epileptic encephalopathy; focal epilepsy; copy number variation; genetic generalized epilepsy