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

Collapse authors list.
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.

Access the full-text of this item by clicking on the Open Access link.

Item Type:	Article
Depositing User:	Symplectic Admin
Date Deposited:	03 Jan 2018 11:41
Last Modified:	12 Apr 2021 19:13
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