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A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood
- 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
Citation
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.
Online issue publication
April 27, 2016
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Copyright 2004 Journal of Medical Genetics