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Showing articles 0 to 6 of 6 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 Abnormal and Persistent Mineralization of Globi Pallidi in GAMT Deficiency Neurol 104:e213636, Chanda,G.,et al, 2025 A 13-Year-Old Boy with Subacute-Onset Spastic Gait JAMA Neurol 78:e1-e2, Xie, N.,et al, 2021 A 13-year-old boy with Chronic Ataxia and Developmental Delay Neurol 88:e116-e121, Libdeh, A.A.,et al, 2017 Diagnostic Exome, Sequencing in Persons with Severe Intellectual Disability NEJM 367:1921-1929, Ligt, J.,et al, 2012 Showing articles 0 to 6 of 6