Recurrent De Novo Mutations of SCN1A in Severe Myoclonic Epilepsy of Infancy

« Previous Next »Pediatric Neurology
Volume 34, Issue 2 , Pages 116-120, February 2006

Jennifer A. Kearney, PhD
- Department of Human Genetics, University of Michigan, Ann Arbor, Michigan
Anna K. Wiste, BS
- Department of Human Genetics, Emory University, Atlanta, Georgia
Ulrich Stephani, MD
- Neuropediatric Department, University Hospital Schlewig-Holstein, Campus Kiel, Kiel, Germany
Michelle M. Trudeau, MS
- Department of Human Genetics, University of Michigan, Ann Arbor, Michigan
Anne Siegel, BS
- Department of Human Genetics, Emory University, Atlanta, Georgia
Rajesh RamachandranNair, MD
- Department of Pediatrics, The Hospital for Sick Children, Toronto, Canada
Roy D. Elterman, MD
- Department of Pediatrics, University of Texas Southwestern Medical School at Dallas, Dallas, Texas
Hiltrud Muhle, MD
- Neuropediatric Department, University Hospital Schlewig-Holstein, Campus Kiel, Kiel, Germany
Juliane Reinsdorf, MD
- Neuropediatric Department, University Hospital Schlewig-Holstein, Campus Kiel, Kiel, Germany
W. Donald Shields, MD
- Department of Pediatrics, University of California at Los Angeles
Miriam H. Meisler, PhD
- Department of Human Genetics, University of Michigan, Ann Arbor, Michigan
Andrew Escayg, PhD
- Department of Human Genetics, Emory University, Atlanta, Georgia
- Communications should be addressed to: Dr. Escayg; Department of Human Genetics; Emory University; 615 Michael Street; Whitehead Building, Suite 301; Atlanta, GA 30322.