Clinical Phenotypes of Different MPZ (P0) Mutations May Include Charcot–Marie–Tooth Type 1B, Dejerine–Sottas, and Congenital Hypomyelination
Titel:
Clinical Phenotypes of Different MPZ (P0) Mutations May Include Charcot–Marie–Tooth Type 1B, Dejerine–Sottas, and Congenital Hypomyelination
Auteur:
Warner, Laura E Hilz, Max J Appel, Stanley H Killian, James M Kolodny, Edwin H Karpati, George Carpenter, Stirling Watters, Gordon V Wheeler, Calvin Witt, David Bodell, Adria Nelis, Eva Van Broeckhoven, Christine Lupski, James R