特異なMRI所見を呈し,プリオン蛋白遺伝子codon180の点変異を認めCreutzfeldt-Jakob病と考えられた1例  [in Japanese] A case of probable Creutzfeldt-Jakob disease with a point mutation of prion protein gene codon 180 and atypical MRI findings  [in Japanese]

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Author(s)

Journal

  • 臨床神経学

    臨床神経学 37(8), 671-674, 1997-08-01

References:  12

Cited by:  4

Codes

  • NII Article ID (NAID)
    10008320114
  • NII NACSIS-CAT ID (NCID)
    AN00253207
  • Text Lang
    JPN
  • Article Type
    Journal Article
  • ISSN
    0009918X
  • Data Source
    CJP  CJPref 
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