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Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients
Depienne, C, Trouillard, O, Saint-Martin, C, Gourfinkel-An, I, Bouteiller, D, Carpentier, W, Keren, B, Abert, B, Gautier, A, Baulac, S, Arzimanoglou, A, Cazeneuve, C, Nabbout, R, LeGuern, EVolume:
46
Language:
english
Journal:
Journal of Medical Genetics
DOI:
10.1136/jmg.2008.062323
Date:
March, 2008
File:
PDF, 2.62 MB
english, 2008