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Clinical correlations of mutations in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancy
Berten P.G.M Ceulemans, Lieve R.F Claes, Lieven G LagaeVolume:
30
Year:
2004
Language:
english
DOI:
10.1016/j.pediatrneurol.2003.10.012
File:
PDF, 170 KB
english, 2004