Frequencies of intron 1 and 22 inversions of factor VIII VIII gene: A first report in Afghan patients with severe haemophilia A

Mousavi S. H.; Mesbah‐Namin S. A.; Rezaie N.; Zeinali S.

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Frequencies of intron 1 and 22 inversions of factor VIII VIII gene: A first report in Afghan patients with severe haemophilia A

机译：因子VIII VIII基因的Intron 1和22逆频率：阿富汗患者严重血梨A的第一报告

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《Haemophilia: the official journal of the World Federation of Hemophilia》 |2018年第3期|共4页
作者
Mousavi S. H.; Mesbah‐Namin S. A.; Rezaie N.; Zeinali S.;
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作者单位

Faculty of Medical SciencesTarbiat Modares UniversityTehran Iran;

Faculty of Medical SciencesTarbiat Modares UniversityTehran Iran;

Faculty of MedicineKhatam‐al‐Nabieen UniversityKabul Afghanistan;

Department of Molecular MedicinePasteur InstituteTehran Iran;

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正文语种 eng
中图分类妇产科学;
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1. Frequencies of intron 1 and 22 inversions of factor VIII VIII gene: A first report in Afghan patients with severe haemophilia A [J] . Mousavi S. H., Mesbah‐Namin S. A., Rezaie N., Haemophilia: the official journal of the World Federation of Hemophilia . 2018,第3期

机译：因子VIII VIII基因的Intron 1和22逆频率：阿富汗患者严重血梨A的第一报告
2. HLA genotype of patients with severe haemophilia A due to intron 22 inversion with and without inhibitors of factor VIII. [J] . Oldenburg J, Picard JK, Schwaab R, Thrombosis and Haemostasis: Journal of the International Society on Thrombosis and Haemostasis . 1997,第2期

机译：重度A型血友病患者的HLA基因型，归因于22内含子倒置，含或不含VIII因子抑制剂。
3. Analysis of intron 1 factor VIII gene inversion for direct diagnosis in patients with severe haemophilia A in China. [J] . Liang Y, Yan M, Xiao B, Prenatal Diagnosis . 2008,第2期

机译：内含子1因子VIII基因倒置分析在中国重症A型血友病患者中的直接诊断
4. Inactiwatlon of Animal Factor VIII by human Factor VIII Inhibitors: Inwestigation of Plasma from Patients with Inhibitors in congenital Hemophilia I and from Patients with acquired Hemophilia A [C] . V. Aumann, G. Lutze (Jr.), G. Lutze (Sen.), Hemophilie-Symposion . 2003

机译：人为因子VIII抑制剂的动物因子VIII的乙酰丁酮：先天性血友病药中抑制剂患者的血浆中的预防
5. Combined deficiency of factors V and VIII by chance coinheritance of parahaemophilia and haemophilia A, but not by mutations of either LMAN1 or MCFD2 [D] . 鈴木幸子 2019

机译：副血友病和A血友病的偶然一致性导致因子V和VIII的联合缺乏，但不是LMAN1或MCFD2的突变
6. Identification of the Intron 22 and Intron 1 Inversions of the Factor VIII Gene in Iraqi Kurdish Patients With Hemophilia A [O] . Aveen M. Raouf Abdulqader, Ali Ibrahim Mohammed, Shwan Rachid, 2020

机译：伊拉克库尔德血友病患者中VIII因子基因的22号内含子和1号内含子1的鉴定。
7. Analysis of intron 22 inversions of the factor VIII gene in severe hemophilia A: implications for genetic counseling [O] . PV Jenkins, PW Collins, E Goldman, 1994

机译：严重血友病中因子VIII基因的Intron 22逆分析A：遗传咨询的影响
8. Influence of Factor VIII/von Willebrand Factor Protein (F VIII/vWF) and F VIII/vWF-Poor Cryoprecipitate on Post-Ischemic Microvascular Reperfusion in the Central Nervous System [R] . Hallenbeck, J. M., Furlow, T. W., Gralnick, H. R. 1980

机译：因子VIII / von Willebrand因子蛋白（F VIII / vWF）和F VIII / vWF-差冷沉淀物对中枢神经系统缺血后微血管再灌注的影响

Frequencies of intron 1 and 22 inversions of factor VIII VIII gene: A first report in Afghan patients with severe haemophilia A

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