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An interstitial duplication at 2q24.3 involving the SCN1A, SCN2A, SCN3A genes associated with infantile epilepsy

Authors

  • Gerald Raymond,

    1. Kennedy Krieger Institute, Baltimore, Maryland
    2. Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland
    3. Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland
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  • Elizabeth Wohler,

    1. Kennedy Krieger Institute, Baltimore, Maryland
    2. Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland
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  • Carolyn Dinsmore,

    1. Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland
    2. McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland
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  • Jeanne Cox,

    1. Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland
    2. McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland
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  • Michael Johnston,

    1. Kennedy Krieger Institute, Baltimore, Maryland
    2. Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland
    3. Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland
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  • Denise Batista,

    1. Kennedy Krieger Institute, Baltimore, Maryland
    2. Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland
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  • Tao Wang

    Corresponding author
    1. Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland
    2. McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland
    • McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, 733 North Broadway, BRB513, Baltimore, MD 21205.
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  • How to Cite this Article: Raymond G, Wohler E, Dinsmore C, Cox J, Johnston M, Batista D, Wang T. 2011. An interstitial duplication at 2q24.3 involving the SCN1A, SCN2A, SCN3A genes associated with infantile epilepsy. Am J Med Genet Part A 155:920–923.

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