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Clinical Phenotypes of Different MPZ (P0) Mutations May Include Charcot–Marie–Tooth Type 1B, Dejerine–Sottas, and Congenital Hypomyelination
Laura E Warner, Max J Hilz, Stanley H Appel, James M Killian, Edwin H Kolodny, George Karpati, Stirling Carpenter, Gordon V Watters, Calvin Wheeler, David Witt, Adria Bodell, Eva Nelis, Christine VanVolume:
17
Year:
1996
Language:
english
DOI:
10.1016/s0896-6273(00)80177-4
File:
PDF, 1.01 MB
english, 1996