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Epilepsy as part of the phenotype associated with ATP1A2 mutations

✍ Scribed by 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; Peter De Jonghe

Book ID: 109110626
Publisher: Wiley (Blackwell Publishing)
Year: 2008
Tongue: English
Weight: 244 KB
Volume: 49
Category: Article
ISSN: 0013-9580
DOI: 10.1111/j.1528-1167.2007.01415.x

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