Nonclassic Steroid 21-Hydroxylase Deficiency due to a Homozygous V281L Mutation in CYP21A2 Detected by the Neonatal Mass-Screening Program in Japan

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著者

    • SHINAGAWA TAKASHI
    • Department of Endocrinology and Metabolism, National Research Institute for Child Health and Development
    • HORIKAWA REIKO
    • Division of Endocrinology and Metabolism, National Center for Child Health and Development
    • ISOJIMA TSUYOSHI
    • Division of Endocrinology and Metabolism, National Center for Child Health and Development
    • NAIKI YASUHIRO
    • Division of Endocrinology and Metabolism, National Center for Child Health and Development
    • TANAKA TOSHIAKI
    • Department of Clinical Laboratory Medicine, National Center for Child Health and Development
    • KATSUMATA NORIYUKI
    • Department of Endocrinology and Metabolism, National Research Institute for Child Health and Development

収録刊行物

  • Endocrine journal  

    Endocrine journal 54(6), 1021-1025, 2007-12-01 

参考文献:  23件

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被引用文献:  1件

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各種コード

  • NII論文ID(NAID)
    10021264156
  • NII書誌ID(NCID)
    AA10901436
  • 本文言語コード
    ENG
  • 資料種別
    NOT
  • ISSN
    09188959
  • データ提供元
    CJP書誌  CJP引用 
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