Reye 症候群で発症した肝型CPT I欠損症のCPT1-A遺伝子の解析  [in Japanese] Mutations of CPT1A gene result in hepatic carnitine palmitoyltransferase I deficiency : cDNA and genomic DNA analysis of a infant presenting with Reye syndrome  [in Japanese]

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Author(s)

Journal

  • 日本先天代謝異常学会雑誌  

    日本先天代謝異常学会雑誌 15(2), 199, 1999-10-22 

References:  1

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Codes

  • NII Article ID (NAID)
    10018938792
  • NII NACSIS-CAT ID (NCID)
    AN10068981
  • Text Lang
    JPN
  • Article Type
    SHO
  • ISSN
    09120122
  • Data Source
    CJP 
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