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Liesbet Deprez, Sarah Weckhuysen, Katelijne Peeters, Tine Deconinck, Kristl G. Claeys, Lieve R.F. Claes, Arvid Suls, Tine Van Dyck, André Palmini, Gert Matthijs, Wim Van Paesschen and Peter De Jonghe Epilepsy as part of the phenotype associated with ATP1A2 mutations Epilepsia 49

Version of Record online: 20 NOV 2007 | DOI: 10.1111/j.1528-1167.2007.01415.x

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