Journal Logo

You can read the full text of this article if you:

Access through Ovid

A novel heterozygous mutation (γIIe367Thr) causes congenital dysfibrinogenemia in a Chinese family

Luo, Shasha; Xu, Qiyu; Xie, Yaosheng; Li, Xiaolong; Jin, Yanhui; Yang, Lihong; Liu, Siqi; Wang, Mingshan

Author Information
Blood Coagulation & Fibrinolysis: December 2020 - Volume 31 - Issue 8 - p 569-574
doi: 10.1097/MBC.0000000000000948
  • Buy


Copyright © 2020 Wolters Kluwer Health, Inc. All rights reserved.