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Showing articles 0 to 3 of 3 Filter Applied: exome sequencing (Click to remove) Heterozygous de-Novo Mutations in ATP1A3 in Patients with Alternating Hemiplegia of Childhood:A Whole-Exome Sequencing Gene-Identification Study Lancet Neurol 11:764-773, Rosewich,H.,et al, 2012 Abnormal and Persistent Mineralization of Globi Pallidi in GAMT Deficiency Neurol 104:e213636, Chanda,G.,et al, 2025 A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements Neurol 103:e210046, Panigrahi,B.,et al, 2024 Showing articles 0 to 3 of 3