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 journalArticle

Original languageEnglish
Pages (from-to)621-628
Number of pages8
JournalJournal of Medical Genetics
Volume41
Issue number8
Publication statusPublished - Aug 2004

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Bassi, M. T., Bresolin, N., Tonelli, A., Nazos, K., Crippa, F., Baschirotto, C., Zucca, C., Bersano, A., Dolcetta, D., Boneschi, F. M., Barone, V., & Casari, G. (2004). A novel mutation in the ATP1A2 genes causes alternating hemiplegia of childhood. Journal of Medical Genetics, 41(8), 621-628.