P23.5 Benign myoclonic epilepsy of infan
P23.5 Benign myoclonic epilepsy of infancy as the initial clinical presentation of a SLC2A1 mutation
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N. Gaspard; A. Suis; C. Vilain; P. De Jonghe; P. van Bogaert
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Article
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2011
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Elsevier Science
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English
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