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

✍ Scribed by K. R. J. Vanmolkot; H. Stroink; J. B. Koenderink; E. E. Kors; J. J. M. W. van den Heuvel; E. H. van den Boogerd; A. H. Stam; J. Haan; B. B. A. De Vries; G. M. Terwindt; R. R. Frants; M. D. Ferrari; A. M. J. M. van den Maagdenberg

Publisher: John Wiley and Sons
Year: 2006
Tongue: English
Weight: 253 KB
Volume: 59
Category: Article
ISSN: 0364-5134
DOI: 10.1002/ana.20760

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