‘Absence of T378N mutation of <i>ATP1A2</i> gene in five patients with alternating hemiplegia of childhood’

Boileau, S; Vuillaume, I; Sablonnière, Bernard; Marignier, S.; Portes, Vincent Des; Vallée, Louis; Auvin, Stéphane

doi:10.1111/j.1469-8749.2008.03111.x

Develop Med Child Neuro

2008

DOI: 10.1111/j.1469-8749.2008.03111.x

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‘Absence of T378N mutation of ATP1A2 gene in five patients with alternating hemiplegia of childhood’

S Boileau¹,

I Vuillaume²,

Bernard Sablonnière³

et al.

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‘Absence of T378N mutation of ATP1A2 gene in five patients with alternating hemiplegia of childhood’

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References 12 publications

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