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

✍ Scribed by S.M. Zuberi; L.H. Eunson; M.G. Hanna; J.B.P. Stephenson; V. Ramesh

Book ID: 114361027
Publisher: Elsevier Science
Year: 1999
Tongue: English
Weight: 142 KB
Volume: 3
Category: Article
ISSN: 1090-3798
DOI: 10.1016/s1090-3798(99)91133-9

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