Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1
Nature Genetics2013Vol. 45(7), pp. 825–830
Citations Over TimeTop 1% of 2013 papers
Gemma L. Carvill, Sinéad B. Heavin, Simone C. Yendle, Jacinta M. McMahon, Brian J. O’Roak, Joseph Cook, Adiba Khan, Michael O. Dorschner, Molly Weaver, Sophie Calvert, Stephen Malone, Geoff Wallace, Thorsten Stanley, Ann M E Bye, Andrew Bleasel, Katherine B. Howell, Sara Kivity, Mark T. Mackay, Victoria Rodriguez‐Casero, Richard Webster, Amos D. Korczyn, Zaid Afawi, Nathanel Zelnick, Tally Lerman‐Sagie, Dorit Lev, Rikke S. Møller, Deepak Gill, Danielle M. Andrade, Jeremy L. Freeman, Lynette G. Sadleir, Jay Shendure, Samuel F. Berkovic, Ingrid E. Scheffer, Heather C. Mefford
Related Papers
- → Etiologic and Pathogenetic Study of Mental Retardation with Multiple Congenital Anomalies(1992)7 cited
- Clinico-Etiological Study Of Urticaria(2004)
- → Clinical characteristics of children with mental retardation of unknown etiology in Korea(1999)2 cited
- → Etiology of Endogenous Uveitis in Childhood(1981)1 cited
- → Etiology(2018)