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Genotype-Phenotype Correlations in a Group of 15 SCN1A-Mutated Italian Patients with GEFS+ Spectrum (Seizures plus, Classical and Borderline Severe Myoclonic Epilepsy of Infancy)
Nicita, F., Spalice, A., Papetti, L., Ursitti, F., Parisi, P., Gennaro, E., Zara, F., Iannetti, P.Volume:
25
Language:
english
Journal:
Journal of Child Neurology
DOI:
10.1177/0883073810365737
Date:
November, 2010
File:
PDF, 150 KB
english, 2010