A POINT MUTATION, C TO T, IN EXON 8 OF THE PORPHOBILINOGEN DEAMINASE GENE IN A JAPANESE FAMILY WITH ACUTE INTERMITTENT PORPHYRIA

この論文をさがす

著者

    • DAIMON Makoto
    • The Third Department of Internal Medicine, Yamagata University School of Medicine
    • YAMATANI Keiichi
    • The Third Department of Internal Medicine, Yamagata University School of Medicine
    • IGARASHI Masahiko
    • The Third Department of Internal Medicine, Yamagata University School of Medicine
    • FUKASE Norio
    • The Third Department of Internal Medicine, Yamagata University School of Medicine
    • OHNUMA Hiroshi
    • The Third Department of Internal Medicine, Yamagata University School of Medicine
    • IKEZAWA Yoshihiro
    • The Third Department of Internal Medicine, Yamagata University School of Medicine
    • SUGIYAMA Kazuhiko
    • The Third Department of Internal Medicine, Yamagata University School of Medicine
    • MANAKA Hideo
    • The Third Department of Internal Medicine, Yamagata University School of Medicine
    • TOMINAGA Makoto
    • The Third Department of Internal Medicine, Yamagata University School of Medicine
    • SASAKI Hideo
    • The Third Department of Internal Medicine, Yamagata University School of Medicine

収録刊行物

  • The Japanese journal of human genetics

    The Japanese journal of human genetics 40(2), 207-213, 1995-06-30

    Japan Society of Human Genetics

参考文献:  22件中 1-22件 を表示

各種コード

  • NII論文ID(NAID)
    10013837730
  • NII書誌ID(NCID)
    AA10830349
  • 本文言語コード
    ENG
  • 資料種別
    SHO
  • ISSN
    09168478
  • NDL 記事登録ID
    3632610
  • NDL 刊行物分類
    SC391(先天異常・奇形)
  • NDL 雑誌分類
    ZS16(科学技術--医学--人類遺伝学)
  • NDL 請求記号
    Z54-H248
  • データ提供元
    CJP書誌  NDL 
ページトップへ