De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies

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Myers, Candace T, McMahon, Jacinta M, Schneider, Amy L, Petrovski, Slave, Allen, Andrew S, Carvill, Gemma L, Zemel, Matthew, Say-Kally, Julia E, LaCroix, Amy J, Heinzen, Erin L et al (show 35 more authors) , Hollingsworth, Georgina, Nikanorova, Marina, Corbett, Mark, Gecz, Jozef, Coman, David, Freeman, Jeremy, Calvert, Sophie, Gill, Deepak, Carney, Patrick, Lerman-Sagie, Tally, Sampaio, Hugo, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Eichler, Evan E, Epstein, Michael P, Glauser, Tracy, Johnson, Michael R, Kuzniecky, Ruben, Marson, Anthony G ORCID: 0000-0002-6861-8806, O'Brien, Terence J, Petrou, Ruth Ottman Stephen, Poduri, Annapurna, Pickrell, William O, Chung, Seo-Kyung, Rees, Mark I, Sherr, Elliott, Sadleir, Lynette G, Goldstein, David B, Lowenstein, Daniel H, Moller, Rikke S, Berkovic, Samuel F, Scheffer, Ingrid E, Mefford, Heather C and Consortium, Epi4K (2016) De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies. AMERICAN JOURNAL OF HUMAN GENETICS, 99 (2). 287 - 298.

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Item Type:	Article
Depositing User:	Symplectic Admin
Date Deposited:	03 Jan 2018 11:41
Last Modified:	13 Jan 2022 15:10
DOI:	10.1016/j.ajhg.2016.06.003
Open Access URL:	http://www.cell.com/ajhg/fulltext/S0002-9297(16)30...
Related URLs:	Author
URI:	https://livrepository.liverpool.ac.uk/id/eprint/3015345