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Showing articles 0 to 3 of 3 Filter Applied: gene mutation (Click to remove) Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease Neurol 92:101-103, Kang, M.J.,et al, 2019 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 Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene NEJM 362:2213-2219, Case 17-2010, 2010 Showing articles 0 to 3 of 3