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Archives de pédiatrie
Volume 20, n° 4
page 429 (avril 2013)
Doi : 10.1016/j.arcped.2013.01.045

Encéphalopathies épileptiques précoces et mutations de novo de KCNQ2 : large spectre phénotypique. Une étude multicentrique de 15 patients

M. Milh a, b, , J. Sutera-Sardo a, N. Boutry-Kryza c, S. Auvin d, C. Mignot e, C. Lacoste a, N. Villeneuve b, A. Roubertie f, M. Carneiro f, A. Kaminska g, C. Altuzzara h, G. Blanchard i, D. Ville i, M.-A. Barthez j, D. Heron d, A. Afenjar d, N. Dorison k, T. Billette l, m, N. Girard a, L. Vercueil a, c, B. Chabrol a, b, G. Lesca c, L. Villard a
a Inserm, U910, Marseille, France 
b Neuropédiatrie, Marseille, France 
c Génétique, hôpital Édouard-Herriot, Bron, France 
d Neuropédiatrie, hôpital Robert Debré, Paris, France 
e Génétique, hôpital Pitié-Salpêtrière, Paris, France 
f Neuropédiatrie et Inserm U1051, INM Montpellier, France 
g Neurophysiologie, hôpital Necker, Paris, France 
h Neuropédiatrie, Besançon, France 
i Neuropédiatrie, hôpital femme-mère-enfant, Bron, France 
j Neuropédiatrie, Tours, France 
k Neuropédiatrie, hôpital Trousseau, Paris, France 
l Neuroradiologie, Marseille, France 
m Neurophysiologie, Grenoble, France 

Auteur correspondant.

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