A novel exon 1 mutation in a patient with atypical lafora progressive myoclonus epilepsy seen as childhood-onset cognitive deficit.
Academic Article
Publication Date:
2004
Iris type:
01.01 Articolo in rivista
List of contributors:
CIRO' CANDIANO, Innocenza; Carrideo, Sara; Quattrone, Aldo; Gambardella, Antonio; Annesi, Grazia; DE MARCO, ELVIRA VALERIA; Spadafora, Patrizia; Annesi, Ferdinanda; Civitelli, Donatella
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