Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation.
until further notice
SourceAnnals of Neurology, 59, 2, (2006), pp. 310-314
Article / Letter to editor
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Annals of Neurology
SubjectDCN 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 disorders
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