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De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies / Candace T. Myers, Jacinta M. McMahon, Amy L. Schneider, Slavé Petrovski, Andrew S. Allen, Gemma L. Carvill, Matthew Zemel, Julia E. Saykally, Amy J. LaCroix, Erin L. Heinzen, Georgina Hollingsworth, Marina Nikanorova, Mark Corbett, Jozef Gecz, David Coman, Jeremy Freeman, Sophie Calvert, Deepak Gill, Patrick Carney, Tally Lerman-Sagie, Hugo Sampaio, Patrick Cossette, Norman Delanty, Dennis Dlugos, Evan E. Eichler, Michael P. Epstein, Tracy Glauser, Michael R. Johnson, Ruben Kuzniecky, Anthony G. Marson, Terence J. O’Brien, Ruth Ottman, Stephen Petrou, Annapurna Poduri, Owen Pickrell, Seo-Kyung Chung, Mark Rees, Elliott Sherr, Lynette G. Sadleir, David B. Goldstein, Daniel H. Lowenstein, Rikke S. Møller, Samuel F. Berkovic, Ingrid E. Scheffer, Heather C. Mefford

The American Journal of Human Genetics, Volume: 99, Issue: 2, Pages: 287 - 298

Swansea University Authors: Owen Pickrell, Seo-Kyung Chung, Mark Rees

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Published in: The American Journal of Human Genetics
ISSN: 0002-9297
Published: Elsevier BV 2016
Online Access: Check full text

URI: https://cronfa.swan.ac.uk/Record/cronfa29412
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College: Swansea University Medical School
Issue: 2
Start Page: 287
End Page: 298