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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