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Showing articles 0 to 2 of 2 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 A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia Neurol 104:e213593, Pence, K.L. &Clark, R.A., 2025 Showing articles 0 to 2 of 2