Protocadherin 19 mutations in girls with infantile-onset epilepsy

C. Marini, D. Mei, Daniele Mei, L. Parmeggiani, V. Norci, E. Calado, A. Ferrari, A. Moreira, T. Pisano, N. Specchio, F. Vigevano, Domenica Immacolata Battaglia, R. Guerrini

Research output: Contribution to journalArticle

105 Citations (Scopus)

Abstract

To explore the causative role of PCDH19 gene (Xq22) in female patients with epilepsy.
Original languageEnglish
Pages (from-to)646-653
Number of pages8
JournalNeurology
Volume75
DOIs
Publication statusPublished - 2010

Keywords

  • Age of Onset
  • Cadherins
  • Electroencephalography
  • Female
  • Humans
  • Infant
  • Magnetic Resonance Imaging
  • Point Mutation
  • Seizures, Febrile

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