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3. Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene. Panagiotakaki E; Tiziano FD; Mikati MA; Vijfhuizen LS; Nicole S; Lesca G; Abiusi E; Novelli A; Di Pietro L; ; ; Harder AVE; Walley NM; De Grandis E; Poulat AL; Portes VD; Lépine A; Nassogne MC; Arzimanoglou A; Vavassori R; Koenderink J; Thompson CH; George AL; Gurrieri F; van den Maagdenberg AMJM; Heinzen EL Eur J Hum Genet; 2024 Feb; 32(2):224-231. PubMed ID: 38097767 [TBL] [Abstract][Full Text] [Related]
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6. 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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