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
小鼠外周髓鞘蛋白P0突变的病理特征与人类夏科-马里-图斯病1B型（Charcot-Marie-Tooth disease 1B）的严重早发型疾病相似。
期刊:Journal of Cell Biology
影响因子:6.4
doi:10.1083/jcb.200402087
Rünker, Annette E; Kobsar, Igor; Fink, Torsten; Loers, Gabriele; Tilling, Thomas; Putthoff, Peggy; Wessig, Carsten; Martini, Rudolf; Schachner, Melitta
