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Copy Number Variant Analysis from Exome Data in 349 Patients with Epileptic Encephalopathy

Bassel Abou-Khalil,Brian K. Alldredge,Andrew S. Allen,Eva Andermann,Frederick Andermann,Dina Amrom,Jocelyn F. Bautista,Samuel F. Berkovic,Alex Boro,Gregory Cascino,Bradley P. Coe,Damian Consalvo,Joseph Cook,Patrick Cossette,Patricia Crumrine,Norman Delanty,Orrin Devinsky,Dennis Dlugos,Evan E. Eichler,Michael P. Epstein,Miguel Fiol,Nathan B. Fountain,Jacqueline French,Daniel Friedman,Eric B. Geller,Tracy Glauser,Simon Glynn,David B. Goldstein,Sheryl R. Haut,Jean Hayward,Erin L. Heinzen,Sandra L. Helmers,Michael R. Johnson,Sucheta Joshi,Andres Kanner,Heidi E. Kirsch,Robert C. Knowlton,Eric H. Kossoff, Nik Krumm,Rachel Kuperman,Ruben Kuzniecky,Daniel H. Lowenstein,Anthony G. Marson,Shannon M. McGuire,Heather C. Mefford,Paul V. Motika,Ben Nelson,Sahar Esmaeeli Nieh,Edward J. Novotny,Terence J. O'Brien,Ruth Ottman,Juliann M. Paolicchi,Jack Parent,Kristen Park,Stephen Petrou,Slave Petrovski,Annapurna Poduri,Archana Raja,Elizabeth K. Ruzzo,Ingrid E. Scheffer,Renee A. Shellhaas,Elliott Sherr,Jerry J. Shih,Rani Singh,Joseph Sirven,Michael C. Smith,Joe Sullivan,Liu Lin Thio,Anu Venkat,Eileen P. G. Vining,Gretchen K. Von Allmen,Judith L. Weisenberg,Peter Widdess-Walsh,Melodie R. Winawer

ANNALS OF NEUROLOGY（2015）

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Key words
Exome Sequencing,Copy Number Variation
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