新生児高ビリルビン血症の一因となるビリルビンUDP-グルクロン酸トランスフェラーゼ遺伝子の変異 : アジア人において高頻度に認められた点突然変異について  [in Japanese] Neonatal hyperbilirubinemia and mutation of the bilirubin uridine diphosphateglucuronosyltansferase gene : A common missense mutation among Asian people  [in Japanese]

Search this Article

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), 176, 1998-10-15 

References:  2

You must have a user ID to see the references.If you already have a user ID, please click "Login" to access the info.New users can click "Sign Up" to register for an user ID.

Codes

  • NII Article ID (NAID)
    10018922061
  • NII NACSIS-CAT ID (NCID)
    AN10068981
  • Text Lang
    JPN
  • Article Type
    SHO
  • ISSN
    09120122
  • Data Source
    CJP 
Page Top