@article{d687a9519d2b496ab0a956a437780e03,
title = "Co-occurring malformations of cortical development and SCN1A gene mutations.",
keywords = "SEVERE MYOCLONIC EPILEPSY, PERIVENTRICULAR NODULAR HETEROTOPIA, REDUCED SODIUM CURRENT, DRAVET SYNDROME, HIPPOCAMPAL SCLEROSIS, NEURONAL MIGRATION, CEREBRAL-CORTEX, MOUSE MODEL, INFANCY, DYSPLASIA",
author = "Carmen Barba and Elena Parrini and Roland Coras and Anna Galuppi and Dana Craiu and Gerhard Kluger and Antonia Parmeggiani and Tom Pieper and Thomas Schmitt-Mechelke and Pasquale Striano and Flavio Giordano and Ingmar Blumcke and Renzo Guerrini",
note = "Paracelsus Medical University Salzburg, Salzburg, Austria",
year = "2014",
doi = "10.1111/epi.12658",
language = "English",
volume = "55",
pages = "1009--1019",
journal = "EPILEPSIA",
issn = "0013-9580",
publisher = "Wiley Verlag ",
number = "7",
}