397 The clinical phenotype of a child with a novel calcium channel gene (CACNA1A) mutation associated with episodic ataxia type 2 and absence epilepsy

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Bibliographic Details
Published inEuropean journal of paediatric neurology Vol. 3; no. 6; p. A55
Main Authors Zuberi, S.M., Eunson, L.H., Hanna, M.G., Stephenson, J.B.P., Ramesh, V.
Format Journal Article
LanguageEnglish
Published Elsevier Ltd 1999
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ISSN:1090-3798
1532-2130
DOI:10.1016/S1090-3798(99)91133-9