A novel mutation in the ATP1A2 genes causes alternating hemiplegia of childhood

M. T. Bassi, N. Bresolin, A. Tonelli, K. Nazos, F. Crippa, C. Baschirotto, C. Zucca, A. Bersano, D. Dolcetta, F. M. Boneschi, V. Barone, G. Casari

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)621-628
Number of pages8
JournalJournal of Medical Genetics
Issue number8
Publication statusPublished - Aug 2004

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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