Genetics and genotype-phenotype correlations in early onset epileptic encephalopathy with burst suppression

Author:

Olson Heather E.12,Kelly McKenna1,LaCoursiere Christopher M.1,Pinsky Rebecca1,Tambunan Dimira1,Shain Catherine13,Ramgopal Sriram14,Takeoka Masanori25,Libenson Mark H.25,Julich Kristina6,Loddenkemper Tobias25,Marsh Eric D.7,Segal Devorah89,Koh Susan10,Salman Michael S.11,Paciorkowski Alex R.12,Yang Edward213,Bergin Ann M.25,Sheidley Beth Rosen1,Poduri Annapurna12

Affiliation:

1. Epilepsy Genetics Program, Department of Neurology, Division of Epilepsy and Clinical Neurophysiology; Boston Children's Hospital; Boston MA

2. Harvard Medical School; Boston MA

3. Center for Human Genetic Research, Massachusetts General Hospital; Boston MA

4. Department of Pediatrics, Children's Hospital of Pittsburgh of UPMC; University of Pittsburgh School of Medicine; Pittsburgh PA

5. Department of Neurology, Division of Epilepsy and Clinical Neurophysiology; Boston Children's Hospital; Boston MA

6. Department of Neurology; Boston Children's Hospital; Boston MA

7. Neurogenetics Program, Department of Neurology; Children's Hospital of Philadelphia; Philadelphia PA

8. Department of Neurology; Rutgers New Jersey Medical School; Newark NJ

9. Department of Pediatrics; Division of Pediatric Neurology, Weill Cornell Medicine; New York NY

10. Department of Pediatrics and Neurology; Children's Hospital of Colorado; Aurora CO

11. Section of Pediatric Neurology, Winnipeg Children's Hospital and Department of Pediatrics and Child Health, College of Medicine, Faculty of Health Sciences; University of Manitoba; Winnipeg Manitoba Canada

12. Departments of Genetics and Neurology; University of Rochester; Rochester NY

13. Department of Radiology; Boston Children's Hospital; Boston MA

Funder

Aaron's Ohtahara Foundation

Dravet Syndrome Foundation

NIH National Institute of Neurological Disorders and Stroke

Child Neurology Foundation

Publisher

Wiley

Subject

Clinical Neurology,Neurology

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