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凝血因子Ⅻ缺乏症一例 被引量:3

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出处 《中华血液学杂志》 CAS CSCD 北大核心 2003年第9期463-463,共1页 Chinese Journal of Hematology
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同被引文献27

  • 1徐方运,田萌苏,田鹏,杨仁池.凝血因子Ⅻ缺乏症一例[J].中华检验医学杂志,2004,27(10):662-662. 被引量:2
  • 2朱文艳,高华强,邹嘉平.凝血因子Ⅻ缺乏一例[J].江苏医药,2005,31(2):118-118. 被引量:2
  • 3王学锋,戴菁,王明山,丁秋兰,王鸿利.两个遗传性凝血因子Ⅻ缺陷症家系FⅫ基因突变分析[J].诊断学理论与实践,2005,4(6):447-450. 被引量:12
  • 4[1]Wachtfogel YT,DeLa Cadena RA,Colman RW.Structural biology,cellular interactions and pathophysiology of the contact system[J].Thromb Res,1993,72(1):1-21.
  • 5[3]Kanaji T,Kanaji S,Osaki K,et al.Identification and characterization of two novel mutations (Q421 K and R123P) in congenital factor Ⅻ deficiency [J].Thromb Haemost,2001,86(6):1409-1415.
  • 6[4]Cool DE,Edgell C J,Louie GV,et al.Characterization of human blood coagulation factor Ⅻ cDNA.Prediction of the primary structure of factor Ⅻ and the tertiary structure of beta-factor Ⅻa [J].J Biol Chem,1985,260(25):13666-13676.
  • 7[5]Kozak M.The scanning model for translation:an update[J].J Cell Biol,1989,108(2):229-241.
  • 8[6]Kanaji T,Okamura T,Osaki K,et al.A common genetic polymorphism (46 C to T substitution) in the 5'-untranslated region of the coagulation factor Ⅻ gene is associated with low translation efficiency and decrease in plasma factor Ⅻ level[J].Blood,1998,91(6):2010-2014.
  • 9[7]Kanaji T,Kanaji S,Osaki K,et al.Identification and characterization of two novel mutations (Q421 K and R123P) in congenital factor Ⅻ deficiency [J].Thromb Haemost,2001,86(6):1409-1415.
  • 10[8]Pearson PL,Van DKJ,Veltkamp J.Reduced Hageman factor level in a 6p-patient [J].Cytogenet Cell Genet,1982,32:309.

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