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

por Rünker, Annette E., Kobsar, Igor, Fink, Torsten, Loers, Gabriele, Tilling, Thomas, Putthoff, Peggy, Wessig, Carsten, Martini, Rudolf, Schachner, Melitta
Publicado 2004