ペルオキシソーム欠損症における9番目の新たな病因遺伝子の解明 : H群患者におけるPEX13遺伝子変異の同定  [in Japanese] PEX13, a new responsible gene for complementation group H of peroxisome biogenesis disorders  [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), 221, 1999-10-22 

References:  3

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Codes

  • NII Article ID (NAID)
    10018938831
  • NII NACSIS-CAT ID (NCID)
    AN10068981
  • Text Lang
    JPN
  • Article Type
    NOT
  • ISSN
    09120122
  • Data Source
    CJP 
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