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Mutations in the D′D3 region of VWF traditionally associated with type 1 VWD lead to quantitative and qualitative deficiencies of VWF

机译：传统上与第1型VWD相关的VWF的D'D3区的突变导致VWF的定量和定性缺陷

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Tara C. White-Adams; Christopher J. Ng; Paula M. Jacobi; Sandra L. Haberichter; Jorge A. Di Paola;
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1. Mutations in the D ' D3 region of VWF traditionally associated with type 1 VWD lead to quantitative and qualitative deficiencies of VWF [J] . White-Adams Tara C., Ng Christopher J., Jacobi PaulaM., Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis . 2016,第Null期

机译：传统上与1型VWD相关的VWF D'D3区突变导致VWF的数量和质量缺陷
2. Mutations in the D ' D3 region of VWF traditionally associated with type 1 VWD lead to quantitative and qualitative deficiencies of VWF [J] . White-Adams Tara C., Ng Christopher J., Jacobi PaulaM., Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis . 2016,第Null期

机译：VWF的D'D3区域中的突变传统上与类型1 VWD相关，导致VWF的定量和定性缺陷
3. Common VWF sequence variants associated with higher VWF and FVIII are less frequent in subjects diagnosed with type 1 VWD [J] . Veronica H. Flood, Jill M. Johnsen, Caroline Kochelek, Research and practice in thrombosis and haemostasis. . 2018,第2期

机译：与较高的VWF和FVIII相关的常见VWF序列变异在诊断为1型VWD的受试者中较不常见
4. Type 2B Mutations Destabilize vWF A1 Domain: A Molecular Dynamics Simulation Study [C] . Liu Guangjian, Fang Ying, Wu Jianhua 5th International Conference on Bioinformatics and Biomedical Engineering . 2011

机译：2B型突变破坏vWF A1域的稳定性：分子动力学模拟研究
5. Adenylosuccinate lyases (ASL) from Bacillus subtilis and Homo sapiens: I. Evaluation of types of interactions in the subunit interface II. Studies of five point mutations and mutant ASL hybrids associated with ASL deficiency [D] . De Zoysa Ariyananda, Lushanti M. 2010

机译：来自枯草芽孢杆菌和智人的腺苷琥珀酸裂合酶（ASL）：I.亚基界面中相互作用类型的评估II。与ASL缺乏有关的五点突变和ASL杂种突变体的研究
6. Mutations in the D’D3 region of VWF traditionally associated with type 1 VWD lead to quantitative and qualitative deficiencies of VWF [O] . Tara C. White-Adams, Christopher J. Ng, Paula M. Jacobi, -1

机译：传统上与1型VWD相关的VWF的D’D3区域突变会导致VWF的数量和质量缺陷
7. Polymorphic variation within the VWF gene contributes to the failure to detect mutations in patients historically diagnosed with type 1 von Willebrand disease from the MCMDM-1VWD cohort [O] . Hampshire, Daniel J., Burghel, George J., Goudemand, Jenny, 2010

机译：VWF基因内的多态性变异导致未能从MCMDM-1VWD队列中历来诊断为1型von Willebrand病的患者中检测突变

Mutations in the D′D3 region of VWF traditionally associated with type 1 VWD lead to quantitative and qualitative deficiencies of VWF

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