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A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood
  1. Correspondence to:
 Dr G Casari
 Dibit-San Raffaele Scientific Institute, Via Olgettina 58, 20132 Milan, Italy; casari.giorgiohsr.it
 Dr M T Bassi
 Laboratory of Molecular Biology, Scientific Institute E. Medea, Via D.L. Monza 20, 23842, Bosisio Parini, Lecco, Italy; mtbassibp.lnf.it
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Citation

Bassi MT, Bresolin N, Tonelli A, et al
A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood

Publication history

  • Received February 12, 2004
  • Accepted March 9, 2004
  • First published July 30, 2004.
  • The name of the tenth author of this paper (Boneschi FM) has been listed incorrectly and should read: Martinelli Boneschi F.

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