A novel fibrinogen gamma-chain mutation, p.Cys165Arg, causes disruption of the γ165Cys–Bβ227Cys disulfide bond and ultimately leads to hypofibrinogenemia-Reference-Cited by-同舟云学术

A novel fibrinogen gamma-chain mutation, p.Cys165Arg, causes disruption of the γ165Cys–Bβ227Cys disulfide bond and ultimately leads to hypofibrinogenemia

Published:2018-12 Issue: Volume:172 Page:128-134
ISSN:0049-3848
Container-title:Thrombosis Research
language:en
Short-container-title:Thrombosis Research

Author:

Zhou WeiJie,Luo Meiling,Yan Jie,Xiang LiQun,Wei AiQiu,Deng Xuelian,Liao Lin,Cheng Peng,Deng Donghong,Lin Faquan^ORCID

Funder

Guangxi Medical University

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Hematology

Reference29 articles.

1. In vitro assembly of the component chains of fibrinogen requires endoplasmic reticulum factors;Roy;J. Biol. Chem.,1996

2. The role of betagamma and alphagamma complexes in the assembly of human fibrinogen;Huang;J. Biol. Chem.,1996

3. Biosynthesis of human fibrinogen. Subunit interactions and potential intermediates in the assembly;Huang;J. Biol. Chem.,1993

4. Hepatic endoplasmic reticulum storage diseases;Callea;Liver Int.,1992

5. Congenital fibrinogen disorders;de Moerloose;Semin. Thromb. Hemost.,2009

Cited by 5 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. Clinical, Laboratory, and Molecular Aspects of Congenital Fibrinogen Disorders;Seminars in Thrombosis and Hemostasis;2024-08-16

2. Mutations Accounting for Congenital Fibrinogen Disorders: An Update;Seminars in Thrombosis and Hemostasis;2022-01-24

3. A novel fibrinogen γ-chain frameshift mutation, p. Cys365Phefs*41, causing hypofibrinogenemia with bleeding phenotype in a Chinese family;Annals of Translational Medicine;2021-08

4. Identification and characterization of novel mutations in Chinese patients with congenital fibrinogen disorders;Blood Cells, Molecules, and Diseases;2021-02

5. Fibrinogen Clauss and prothrombin time derived method ratio can differentiate dysfibrinogenemia from hypofibrinogenemia and hyperfibrinogenemia;Thrombosis Research;2020-10