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Research Article

A Role of SCN9A in Human Epilepsies, As a Cause of Febrile Seizures and As a Potential Modifier of Dravet Syndrome

  • Nanda A. Singh mail,

    nsingh@genetics.utah.edu

    Affiliation: Department of Human Genetics, University of Utah, Salt Lake City, Utah, United States of America

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  • Chris Pappas,

    Affiliation: Department of Human Genetics, University of Utah, Salt Lake City, Utah, United States of America

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  • E. Jill Dahle,

    Affiliation: Department of Human Genetics, University of Utah, Salt Lake City, Utah, United States of America

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  • Lieve R. F. Claes,

    Affiliation: VIB Department of Molecular Genetics, University of Antwerp, Antwerp, Belgium

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  • Timothy H. Pruess,

    Affiliation: Department of Pharmacology and Toxicology, Anticonvulsant Drug Development Program, University of Utah, Salt Lake City, Utah, United States of America

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  • Peter De Jonghe,

    Affiliation: VIB Department of Molecular Genetics, University of Antwerp, Antwerp, Belgium

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  • Joel Thompson,

    Affiliation: Division of Pediatric Neurology, University of Utah, Salt Lake City, Utah, United States of America

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  • Missy Dixon,

    Affiliation: Department of Human Genetics, University of Utah, Salt Lake City, Utah, United States of America

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  • Christina Gurnett,

    Affiliation: Department of Neurology, Washington University School of Medicine, St. Louis, Missouri, United States of America

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  • Andy Peiffer,

    Affiliation: Division of Medical Genetics, University of Utah, Salt Lake City, Utah, United States of America

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  • H. Steve White,

    Affiliation: Department of Pharmacology and Toxicology, Anticonvulsant Drug Development Program, University of Utah, Salt Lake City, Utah, United States of America

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  • Francis Filloux,

    Affiliation: Division of Pediatric Neurology, University of Utah, Salt Lake City, Utah, United States of America

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  • Mark F. Leppert

    Affiliation: Department of Human Genetics, University of Utah, Salt Lake City, Utah, United States of America

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  • Published: September 18, 2009
  • DOI: 10.1371/journal.pgen.1000649

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