Clinical Phenotypes of Different MPZ (P0) Mutations May Include Charcot–Marie–Tooth Type 1B, Dejerine–Sottas, and Congenital Hypomyelination

Laura E. Warner(Baylor College of Medicine), Max J. Hilz(Friedrich-Alexander-Universität Erlangen-Nürnberg), Stanley H. Appel(Baylor College of Medicine), James M. Killian(Baylor College of Medicine), Edwin H. Kolodny(New York University), George Karpati(Montreal Neurological Institute and Hospital), Stirling Carpenter(Toronto Western Hospital), Gordon V. Watters(Montreal Children's Hospital), Calvin Wheeler(Kaiser Permanente), David R. Witt(Kaiser Permanente), Adria Bodell(Kaiser Permanente), Eva Nelis(University of Antwerp), Christine Van Broeckhoven(University of Antwerp), James R. Lupski(Baylor College of Medicine)
Neuron
September 1, 1996
10.1016/s0896-6273(00)80177-4
Cited by 363Open Access
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