Severe coagulation factor VII deficiency caused by a novel homozygous mutation (p. Trp284Gly) in loop 140s-Reference-Cited by-同舟云学术

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Severe coagulation factor VII deficiency caused by a novel homozygous mutation (p. Trp284Gly) in loop 140s

Published:2016-06 Issue:4 Volume:27 Page:461-463
ISSN:0957-5235
Container-title:Blood Coagulation & Fibrinolysis
language:en
Short-container-title:

Author:

Hao Xiuping,Cheng XiaoLi,Ye Jiajia,Wang Yingyu,Yang LiHong,Wang Mingshan,Jin Yanhui

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Hematology,General Medicine

Reference11 articles.

1. Isolation and characterization of human factor VII. Activation of factor VII by factor Xa;Bajaj;J Biol Chem,1981

2. Molecular characterization of four novel mutations causing factor VII deficiency;Tamary;Hematol J,2000

3. A novel homozygous missense in the factor VII gene of severe factor in VII deficiency a newborn baby;Lee;Blood Coagul Fibrinolysis,2009

4. Homozygous 2 bp deletion in the human factor VII gene: a nonlethal mutation that is associated with a complete absence of circulating factor VII;Peyvandi;Thromb Haemost,2000

5. Factor VII deficiency;Mariani;Semin Thromb Hemost,2009

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Rare bleeding disorders and advances in gene therapy;Blood Coagulation & Fibrinolysis;2019-12

2. Inï¿½vitro expression of mutant factor VII proteins and characterization of their clinical significance;Molecular Medicine Reports;2017-11-27

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