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Showing articles 0 to 3 of 3 Filter Applied: next-generation sequencing (Click to remove) Clinical Manifestations and Diagnostic Challenges in a 16-Year-Old With Early-Onset Ataxia Neurol 104:e210253, Chadha,D.,et al, 2024 SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases Eur J Hum Genet 24:1016-1021, Choquet,K.,et al, 2016 Molecular and Neurological Features of MELAS Syndrome in Paediatric Patients: A Case Series and Review of the Literature Mal Genet Genomic Med 10:e1955, Seed,L.M.,et al, 2022 Showing articles 0 to 3 of 3