Co-occurring malformations of cortical development and SCN1A gene mutations.

Carmen Barba, Elena Parrini, Roland Coras, Anna Galuppi, Dana Craiu, Gerhard Kluger (Co-author), Antonia Parmeggiani, Tom Pieper, Thomas Schmitt-Mechelke, Pasquale Striano, Flavio Giordano, Ingmar Blumcke, Renzo Guerrini

    Research output: Contribution to journalOriginal Articlepeer-review

    79 Citations (Web of Science)
    Original languageEnglish
    Pages (from-to)1009-1019
    JournalEPILEPSIA
    Volume55
    Issue number7
    DOIs
    Publication statusPublished - 2014

    Keywords

    • SEVERE MYOCLONIC EPILEPSY
    • PERIVENTRICULAR NODULAR HETEROTOPIA
    • REDUCED SODIUM CURRENT
    • DRAVET SYNDROME
    • HIPPOCAMPAL SCLEROSIS
    • NEURONAL MIGRATION
    • CEREBRAL-CORTEX
    • MOUSE MODEL
    • INFANCY
    • DYSPLASIA

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