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

  • N. Hattori, M. Yamamoto, T. Yoshihara, H. Koike, M. Nakagawa, H. Yoshikawa, A. Ohnishi, K. Hayasaka, O. Onodera, M. Baba, H. Yasuda, T. Saito, K. Nakashima, J.-i. Kira, R. Kaji, N. Oka, G. Sobue, Study Group for Hereditary Neuropathy
  • Brain, January 2003, Oxford University Press (OUP)
  • DOI: 10.1093/brain/awg012

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The following have contributed to this page: Dr Osamu Onodera and Professor Kazuhiko Watabe

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