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Showing articles 0 to 3 of 3 Filter Applied: exome sequencing (Click to remove) A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025 SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases Eur J Hum Genet 24:1016-1021, Choquet,K.,et al, 2016 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 Showing articles 0 to 3 of 3