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A novel exon 1 mutation in a patient with atypical lafora progressive myoclonus epilepsy seen as childhood-onset cognitive deficit.

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Description scientific article published in March 2004
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author: Antonio Gambardella  Aldo Quattrone  Sara Carrideo  Donatella Civitelli  Mario Zappia  Grazia Annesi  Elvira Valeria De Marco  Patrizia Tarantino  Rita Barone 

Publication date March 1, 2004
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