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De novo mutation (Arg98→Cys) of the myelin P0 gene and uncompaction of the major dense line of the myelin sheath in a severe variant of Charcot–Marie–Tooth disease type 1B

✍ Scribed by Atsushi Komiyama; Akio Ohnishi; Katsuhiko Izawa; Shunji Yamamori; Hirofumi Ohashi; Osamu Hasegawa

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