ミトコンドリアDNA 8993 T to C変異をみとめたNARP (neurogenic muscle weakness, ataxia, and retinitis pigmentosa)の1例  [in Japanese] A case of NARP (neurogenic muscle weakness, ataxia, and retinitis pigmentosa) with a T-to-C point mutation at nt 8993 of mitochondrial DNA  [in Japanese]

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Author(s)

Journal

  • 臨床神経学

    臨床神経学 40(6), 600-604, 2000-06-01

References:  12

Cited by:  2

Codes

  • NII Article ID (NAID)
    10008309739
  • NII NACSIS-CAT ID (NCID)
    AN00253207
  • Text Lang
    JPN
  • Article Type
    Journal Article
  • ISSN
    0009918X
  • Data Source
    CJP  CJPref 
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