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SCN8A encephalopathy: Research progress and prospects
Authors:Michael F Hammer  Brandy E Fureman  William D Gaillard  Alan L Goldin  Shinichi Hirose  Atsushi Ishii  Barbara L Kroner  Christoph Lossin  Heather C Mefford  Jack M Parent  Manoj Patel  John Schreiber  Randall Stewart  Vicky Whittemore  Karen Wilcox  Jacy L Wagnon  Phillip L Pearl  Ingrid E Scheffer
Institution:1. ARL Division of Biotechnology, University of Arizona, Tucson, Arizona, U.S.A;2. National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, U.S.A;3. Department of Neurology, Children's National Health System, Washington, District of Columbia, U.S.A;4. Center for Neuroscience Research, Children's National Health System, Washington, District of Columbia, U.S.A;5. Microbiology & Molecular Genetics and Anatomy & Neurobiology, University of California, Irvine, California, U.S.A;6. Department of Pediatrics, Fukuoka University School of Medicine, Fukuoka, Japan;7. Biostatistics and Epidemiology, RTI International, Rockville, Maryland, U.S.A;8. Department of Neurology, School of Medicine, University of California Davis, Sacramento, California, U.S.A;9. Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, Washington, U.S.A;10. Department of Neurology, University of Michigan Medical Center and VA Ann Arbor Healthcare System, Ann Arbor, Michigan, U.S.A;11. Department of Anesthesiology, University of Virginia Health System, Charlottesville, Virginia, U.S.A;12. Anticonvulsant Drug Development Program, Department of Pharmacology and Toxicology, University of Utah, Salt Lake City, Utah, U.S.A;13. Department of Human Genetics, University of Michigan, Ann Arbor, Michigan, U.S.A;14. Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, U.S.A
Abstract:
Keywords:Encephalopathy  Bioregistry  Nav1  6  Sodium channel  Mutation  Drug screening     SCN8A   
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