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Whole-Genome Sequencing in a Patient with Charcot-Marie-Tooth Neuropathy
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PCR-Based Strategy for Dx of Hered Neuropathy with Liability to Pressure Palsies & Charcot-Marie-Tooth Dis Type 1A
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Detection of a Varient Protein in Hair:New Diagnostic Method in Portuguese Type Familial Amyloid Polyneuropathy
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Clin Electrophy & Molec Correl in 13 Families with Hered Neurop with Liabil to Press Palsies & Chromosome 17p11. 2 Deletion
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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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Validation of the 2023 International Diagnostic Criteria for MOGAD in a Selected Cohort of Adults and Children
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