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Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation

K R J Vanmolkot1, H Stroink, J B Koenderink

  • 1Department of Human Genetics, Leiden University Medical Centre, Leiden, The Netherlands.

Annals of Neurology
|January 27, 2006
PubMed
Abstract

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