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.
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G. Sobue | K. Nakashima | J. Kira | A. Ohnishi | R. Kaji | M. Nakagawa | H. Yoshikawa | M. Baba | K. Hayasaka | H. Yasuda | O. Onodera | N. Oka | H. Koike | Masahiko Yamamoto | N. Hattori | Toyokazu Saito | T. Yoshihara