Rare Deletions at 16p13.11 Predispose to a Diverse Spectrum of Sporadic Epilepsy Syndromes

✍ Scribed by Erin L. Heinzen; Rodney A. Radtke; Thomas J. Urban; Gianpiero L. Cavalleri; Chantal Depondt; Anna C. Need; Nicole M. Walley; Paola Nicoletti; Dongliang Ge; Claudia B. Catarino; John S. Duncan; Dalia Kasperavičiūte˙; Sarah K. Tate; Luis O. Caboclo; Josemir W. Sander; Lisa Clayton; Kristen N. Linney; Kevin V. Shianna; Curtis E. Gumbs; Jason Smith; Kenneth D. Cronin; Jessica M. Maia; Colin P. Doherty; Massimo Pandolfo; David Leppert; Lefkos T. Middleton; Rachel A. Gibson; Michael R. Johnson; Paul M. Matthews; David Hosford; Reetta Kälviäinen; Kai Eriksson; Anne-Mari Kantanen; Thomas Dorn; Jörg Hansen; Günter Krämer; Bernhard J. Steinhoff; Heinz-Gregor Wieser; Dominik Zumsteg; Marcos Ortega; Nicholas W. Wood; Julie Huxley-Jones; Mohamad Mikati; William B. Gallentine; Aatif M. Husain; Patrick G. Buckley; Ray L. Stallings; Mihai V. Podgoreanu; Norman Delanty; Sanjay M. Sisodiya; David B. Goldstein

• Book ID: 113422835
• Publisher: American Society of Human Genetics
• Year: 2010
• Tongue: English
• Weight: 692 KB
• Volume: 86
• Category: Article
• ISSN: 0002-9297
• DOI: 10.1016/j.ajhg.2010.03.018