Pathology of a mouse mutation in peripheral myelin protein P0 is characteristic of a severe and early onset form of human Charcot-Marie-Tooth type 1B disorder

Annette E. Rünker, Igor Kobsar, Torsten Fink, Gabriele Loers, Thomas Tilling, Peggy Putthoff, Carsten Wessig, Rudolf Martini, Melitta Schachner

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