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

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Publication year
2006
Author(s)
Vanmolkot, K.R.
Stroink, H.
Koenderink, J.B.
Kors, E.E.
Heuvel, J.J.M.W. van den
Boogerd, E.H. van den
Stam, A.H.
Haan, J.H.A. de
Vries, B. de
Terwindt, G.M.
Source
Annals of Neurology, 59, 2, (2006), pp. 310-314
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Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/49308   https://hdl.handle.net/2066/49308
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