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22. Familial Ohtahara syndrome due to a novel ARX gene mutation. Giordano L; Sartori S; Russo S; Accorsi P; Galli J; Tiberti A; Bettella E; Marchi M; Vignoli A; Darra F; Murgia A; Bernardina BD Am J Med Genet A; 2010 Dec; 152A(12):3133-7. PubMed ID: 21108397 [TBL] [Abstract][Full Text] [Related]
23. Mouse orthologue of ARX, a gene mutated in several X-linked forms of mental retardation and epilepsy, is a marker of adult neural stem cells and forebrain GABAergic neurons. Colombo E; Galli R; Cossu G; Gécz J; Broccoli V Dev Dyn; 2004 Nov; 231(3):631-9. PubMed ID: 15376319 [TBL] [Abstract][Full Text] [Related]
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29. ARX mutation c.428-451dup (24bp) in a Brazilian family with X-linked mental retardation. Gestinari-Duarte Rde S; Santos-Rebouças CB; Boy RT; Pimentel MM Eur J Med Genet; 2006; 49(3):269-75. PubMed ID: 16762829 [TBL] [Abstract][Full Text] [Related]
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33. Combination of infantile spasms, non-epileptic seizures and complex movement disorder: a new case of ARX-related epilepsy. Poirier K; Eisermann M; Caubel I; Kaminska A; Peudonnier S; Boddaert N; Saillour Y; Dulac O; Souville I; Beldjord C; Lascelles K; Plouin P; Chelly J; Bahi-Buisson N Epilepsy Res; 2008 Aug; 80(2-3):224-8. PubMed ID: 18468866 [TBL] [Abstract][Full Text] [Related]
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