Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): A clinicopathological study of 205 Japanese patients

Naoki Hattori, Masahiko Yamamoto, Tsuyoshi Yoshihara, Haruki Koike, Masanori Nakagawa, Hiroo Yoshikawa, Akio Ohnishi, Kiyoshi Hayasaka, Osamu Onodera, Masayuki Baba, Hitoshi Yasuda, Toyokazu Saito, Kenji Nakashima, Jun ichi Kira, Ryuji Kaji, Nobuyuki Oka, Gen Sobue, Ichiro Akiguchi, Saburo Sakota, Kiichiro MatsumuraSatoshi Onodera, Shu ichi Ikeda, Takashi Yamamura, Yukio Ando, Masamitsu Nakazato, Kazuhiro Ikenaka, Keiji Wada, Kazuhiko Watabe, Eiko Ando

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