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4. A novel ATP1A3 mutation with unique clinical presentation. Rosewich H; Baethmann M; Ohlenbusch A; Gärtner J; Brockmann K J Neurol Sci; 2014 Jun; 341(1-2):133-5. PubMed ID: 24713507 [TBL] [Abstract][Full Text] [Related]
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11. Alternating Hemiplegia of Childhood: Understanding the Genotype-Phenotype Relationship of ATP1A3 Variations. Capuano A; Garone G; Tiralongo G; Graziola F Appl Clin Genet; 2020; 13():71-81. PubMed ID: 32280259 [TBL] [Abstract][Full Text] [Related]
12. Alternating hemiplegia of childhood in Denmark: clinical manifestations and ATP1A3 mutation status. Hoei-Hansen CE; Dali CÍ; Lyngbye TJ; Duno M; Uldall P Eur J Paediatr Neurol; 2014 Jan; 18(1):50-4. PubMed ID: 24100174 [TBL] [Abstract][Full Text] [Related]
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