P.062 Normal NCS in 42-year-old man with PMP22 duplication

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1. 1Genetic spectrum and clinical features of PMP22 point mutations in Japanese Charcot–Marie–Tooth disease2026 · 1 citations
2. 2Peripheral Myelin Protein-22 and Its Prominence in Charcot-Marie-Tooth Disease2026 · 1 citations
3. 3Hereditary neuropathies caused by mutations in the gene encoding peripheral myelin protein 222025
4. 4Delayed Genetic Diagnosis of a Rare Presentation of Overlapping Peripheral Myelin Protein 22 (PMP22) Neuropathies2026
5. 5Aberrant Molecular Myelin Architecture in Charcot-Marie-Tooth Disease Type 1A and Hereditary Neuropathy with Liability to Pressure Palsies2024