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

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Publication year
2006Source
Annals of Neurology, 59, 2, (2006), pp. 310-314ISSN
Publication type
Article / Letter to editor

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Organization
Pharmacology-Toxicology
Radiology
Human Genetics
Former Organization
Pharmacology/Toxicology
Journal title
Annals of Neurology
Volume
vol. 59
Issue
iss. 2
Page start
p. 310
Page end
p. 314
Subject
DCN 2: Functional Neurogenomics; IGMD 3: Genomic disorders and inherited multi-system disorders; N4i 1: Pathogenesis and modulation of inflammation; N4i 3: Poverty-related infectious diseases; NCMLS 5: Membrane transport and intracellular motility; UMCN 5.1: Genetic defects of metabolism; UMCN 5.4: Renal disordersThis item appears in the following Collection(s)
- Academic publications [204981]
- Electronic publications [103219]
- Faculty of Medical Sciences [81051]
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