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Annals of Neurology|January 27, 2006
Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutationK R J Vanmolkot, H Stroink, J B Koenderink, et al.
Neurology|December 7, 2007
Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraineB de Vries, T Freilinger, K R J Vanmolkot, et al.
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