新生児黄疸と Gilbert 症候群 : 日本人に共通なビリルビンUDP-グルクロン酸トランスフェラーゼ遺伝子変異について  [in Japanese] Neonatal hyperbilirubinemia and Gilbert syndrome : A common mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene among Japanese  [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 14(2), 175, 1998-10-15 

References:  1

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Codes

  • NII Article ID (NAID)
    10018922059
  • NII NACSIS-CAT ID (NCID)
    AN10068981
  • Text Lang
    JPN
  • Article Type
    SHO
  • ISSN
    09120122
  • Data Source
    CJP 
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