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 Van Broeckhoven, James R. Lupski

Research output: Contribution to journal › Article › peer-review

337 Scopus citations

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