(Q28217188)
Statements
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 (English)
Naoki Hattori
Gen Sobue
Toyokazu Saito
Masahiko Yamamoto
Tsuyoshi Yoshihara
Masanori Nakagawa
Hiroo Yoshikawa
Akio Ohnishi
Kiyoshi Hayasaka
Masayuki Baba
Hitoshi Yasuda
Kenji Nakashima
Jun-ichi Kira
Ryuji Kaji
Nobuyuki Oka
Study Group for Hereditary Neuropathy in Japan
Identifiers
2 references
2 references