Journal article 1764 views 170 downloads
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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DOI (Published version): 10.1016/j.ajhg.2016.06.003
Abstract
De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies
Published in: | The American Journal of Human Genetics |
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ISSN: | 0002-9297 |
Published: |
Elsevier BV
2016
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Online Access: |
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URI: | https://cronfa.swan.ac.uk/Record/cronfa29412 |
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College: |
Faculty of Medicine, Health and Life Sciences |
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Issue: |
2 |
Start Page: |
287 |
End Page: |
298 |