Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 <i>ATP1A2</i> mutation - Concepedia

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

83

Citations

29

References

2006

Year

Kaate R. J. Vanmolkot, Hans Stroink, Jan B. Koenderink, E. E. Kors, Jeroen J. M. W. van den Heuvel, Eelke H van den Boogerd, Amber H. van der Stam, J. Haan, Bert B.A. de Vries, Gisela M. Terwindt,

Annals of Neurology

Abstract

Permanent mental retardation in children may be caused by ATP1A2 mutations.

References

	Year	Citations

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