重症の臨床型を呈し,髄鞘Po蛋白がVal 146Phe変異を示したCharcot-Marie-Tooth病1Bの1例  [in Japanese] A case of Charcot-Marie-Tooth disease 1B with Val 146Phe mutation of myelin protein zero showing a severe clinical phenotype  [in Japanese]

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Author(s)

    • 大西 晃生 OHNISHI Akio
    • 産業医科大学神経内科学教室 Department of Neurology, University of Occupational and Environmental Health
    • 青木 朝海 AOKI Asami
    • 産業医科大学神経内科学教室 Department of Neurology, University of Occupational and Environmental Health
    • 辻 貞俊 TSUJI Sadatoshi
    • 産業医科大学神経内科学教室 Department of Neurology, University of Occupational and Environmental Health

Journal

  • 臨床神経学

    臨床神経学 40(3), 268-270, 2000-03-01

References:  10

Codes

  • NII Article ID (NAID)
    10008309010
  • NII NACSIS-CAT ID (NCID)
    AN00253207
  • Text Lang
    JPN
  • Article Type
    SHO
  • ISSN
    0009918X
  • Data Source
    CJP 
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