Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation (Q28293829)

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Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation
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    Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation (English)
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    K R J Vanmolkot
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    H Stroink
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    J B Koenderink
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    E E Kors
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    J J M W van den Heuvel
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    E H van den Boogerd
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    A H Stam
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    J Haan
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    B B A De Vries
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    G M Terwindt
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    R R Frants
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    A M J M van den Maagdenberg
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    February 2006
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    59
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    2
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    310-4
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