Clinical Phenotypes of Different MPZ (P0) Mutations May Include Charcot–Marie–Tooth Type 1B, Dejerine–Sottas, and Congenital Hypomyelination
Open Access
- 1 September 1996
- Vol. 17 (3), 451-460
- https://doi.org/10.1016/s0896-6273(00)80177-4
Abstract
No abstract availableKeywords
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