Ultra-rare genetic variation in common epilepsies: a case-control sequencing study

The Lancet Neurology

Volumn 16, Issue 2, 2017, Pages 135-143

  Allen, Andrew S ^a   Bellows, Susannah T ^a   Berkovic, Samuel F ^a   Bridgers, Joshua ^a   Burgess, Rosemary ^a   Cavalleri, Gianpiero ^a   Chung, Seo Kyung ^a   Cossette, Patrick ^a   Delanty, Norman ^a   Dlugos, Dennis ^a   Epstein, Michael P ^a   Freyer, Catharine ^a   Goldstein, David B ^a   Heinzen, Erin L ^a   Hildebrand, Michael S ^a   Johnson, Michael R ^a   Kuzniecky, Ruben ^a   Lowenstein, Daniel H ^a   Marson, Anthony G ^a   Mayeux, Richard ^a   Mebane, Caroline ^a   Mefford, Heather C ^a   O'Brien, Terence J ^a   Ottman, Ruth ^a   Petrou, Steven ^a   Petrovski, Slavé ^a   Pickrell, William O ^a   Radtke, Rodney A ^a   Rees, Mark I ^a   Regan, Brigid M ^a   Ren, Zhong ^a   Scheffer, Ingrid E ^a   Sills, Graeme J ^a   Thomas, Rhys H ^a   Wang, Quanli ^a   Abou Khalil, Bassel ^a   Alldredge, Brian K ^a   Amrom, Dina ^a   Andermann, Eva ^a   Andermann, Frederick ^a   Bautista, Jocelyn F ^a   Bluvstein, Judith ^a   Boro, Alex ^a   Cascino, Gregory D ^a   Consalvo, Damian ^a   Crumrine, Patricia ^a   Devinsky, Orrin ^a   Fiol, Miguel ^a   Fountain, Nathan B ^a   French, Jacqueline ^a   Friedman, Daniel ^a   Geller, Eric B ^a   Glauser, Tracy ^a   Glynn, Simon ^a   Haas, Kevin ^a   Haut, Sheryl R ^a   Hayward, Jean ^a   Helmers, Sandra L ^a   Joshi, Sucheta ^a   Kanner, Andres ^a   Kirsch, Heidi E ^a   Knowlton, Robert C ^a   Kossoff, Eric H ^a   Kuperman, Rachel ^a   Motika, Paul V ^a   Novotny, Edward J ^a   Paolicchi, Juliann M ^a   Parent, Jack M ^a   Park, Kristen ^a   Poduri, Annapurna ^a   Sadleir, Lynette G ^a   Shellhaas, Renée A ^a   Sherr, Elliott H ^a   Shih, Jerry J ^a   Shinnar, Shlomo ^a   Singh, Rani K ^a   Sirven, Joseph ^a   Smith, Michael C ^a   Sullivan, Joseph ^a   Thio, Liu Lin ^a   Venkat, Anu ^a   Vining, Eileen P G ^a   Von Allmen, Gretchen K ^a   Weisenberg, Judith L ^a   Widdess Walsh, Peter ^a   Winawer, Melodie R ^a   more..

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE CONTROL STUDY; CONTROLLED STUDY; DOMINANT INHERITANCE; EPILEPSY; EXOME; FAMILIAL GENETIC GENERALISED EPILEPSY; FAMILIAL NON ACQUIRED FOCAL EPILEPSY; GENE DELETION; GENE SEQUENCE; GENETIC RISK; GENETIC VARIATION; HETEROZYGOTE; HUMAN; MAJOR CLINICAL STUDY; MULTICENTER STUDY; PRIORITY JOURNAL; RISK ASSESSMENT; DNA SEQUENCE; FOCAL EPILEPSY; GENERALIZED EPILEPSY; GENETIC PREDISPOSITION; GENETICS;

CASE-CONTROL STUDIES; EPILEPSIES, PARTIAL; EPILEPSY, GENERALIZED; EXOME; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; HUMANS; SEQUENCE ANALYSIS, DNA;

EID: 85009876921     PISSN: 14744422     EISSN: 14744465     Source Type: Journal    
DOI: 10.1016/S1474-4422(16)30359-3     Document Type: Article

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