{"publist_id":"5323","status":"public","issue":"1","date_updated":"2021-01-12T06:53:13Z","type":"journal_article","quality_controlled":0,"page":"9 - 11","date_created":"2018-12-11T11:54:01Z","intvolume":" 80","citation":{"ista":"Novarino G, Baek S, Gleeson J. 2013. The sacred disease: The puzzling genetics of epileptic disorders. Neuron. 80(1), 9–11.","apa":"Novarino, G., Baek, S., & Gleeson, J. (2013). The sacred disease: The puzzling genetics of epileptic disorders. Neuron. Elsevier. https://doi.org/10.1016/j.neuron.2013.09.019","ieee":"G. Novarino, S. Baek, and J. Gleeson, “The sacred disease: The puzzling genetics of epileptic disorders,” Neuron, vol. 80, no. 1. Elsevier, pp. 9–11, 2013.","chicago":"Novarino, Gaia, Seungtae Baek, and Joseph Gleeson. “The Sacred Disease: The Puzzling Genetics of Epileptic Disorders.” Neuron. Elsevier, 2013. https://doi.org/10.1016/j.neuron.2013.09.019.","short":"G. Novarino, S. Baek, J. Gleeson, Neuron 80 (2013) 9–11.","mla":"Novarino, Gaia, et al. “The Sacred Disease: The Puzzling Genetics of Epileptic Disorders.” Neuron, vol. 80, no. 1, Elsevier, 2013, pp. 9–11, doi:10.1016/j.neuron.2013.09.019.","ama":"Novarino G, Baek S, Gleeson J. The sacred disease: The puzzling genetics of epileptic disorders. Neuron. 2013;80(1):9-11. doi:10.1016/j.neuron.2013.09.019"},"volume":80,"_id":"1790","publisher":"Elsevier","date_published":"2013-10-02T00:00:00Z","publication":"Neuron","author":[{"last_name":"Novarino","full_name":"Gaia Novarino","id":"3E57A680-F248-11E8-B48F-1D18A9856A87","orcid":"0000-0002-7673-7178","first_name":"Gaia"},{"first_name":"Seungtae","full_name":"Baek, SeungTae","last_name":"Baek"},{"last_name":"Gleeson","full_name":"Gleeson, Joseph G","first_name":"Joseph"}],"day":"02","doi":"10.1016/j.neuron.2013.09.019","extern":1,"month":"10","title":"The sacred disease: The puzzling genetics of epileptic disorders","year":"2013","abstract":[{"lang":"eng","text":"In the September 12, 2013 issue of Nature, the Epi4K Consortium (. Allen etal., 2013) reported sequencing 264patient trios with epileptic encephalopathies. The Consortium focused on genes exceptionally intolerant to sequence variations and found substantial interconnections with autism and intellectual disability gene networks."}],"publication_status":"published"}