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

収録刊行物

• Brain

  Brain 126 (1), 134-151, 2003-01-01

  Oxford University Press (OUP)

キーワード

• Neurology (clinical)

詳細情報

• CRID: 1361137045818811904
• NII論文ID: 30018522869
• DOI: 10.1093/brain/awg012
• ISSN: 14602156
• ISSN: 00068950
• ISSN: http://id.crossref.org/issn/00068950
• Web Site: http://academic.oup.com/brain/article-pdf/126/1/134/848484/awg012.pdf
• データソース種別:
  • Crossref
  • CiNii Articles