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 (Q28217188)
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scientific article (publication date: 2003)
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 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 |
scientific article (publication date: 2003) |
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
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
1 January 2003
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