Identification and characterization of novel mutations in Chinese patients with congenital fibrinogen disorders-Reference-Cited by-同舟云学术

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Identification and characterization of novel mutations in Chinese patients with congenital fibrinogen disorders

Published:2021-02 Issue: Volume:86 Page:102489
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Zhou Puhui,Yu Man,Peng Yan,Ma Pengpeng,Wan Lagen

Funder

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference24 articles.

1. Fibrinogen assembly and secretion. Role of intrachain disulfide loops;Zhang;J. Biol. Chem.,1996

2. A model from electron microscopy for the molecular structure of fibrinogen and fibrin;Weisel;Nature,1981

3. Fibrinogen brescia: hepatic endoplasmic reticulum storage and hypofibrinogenemia because of a gamma284 Gly-->Arg mutation;Brennan;Am. J. Pathol.,2000

4. Fibrinogen angers with a new deletion (gamma GVYYQ 346-350) causes hypofibrinogenemia with hepatic storage;Dib;J. Thromb. Haemost.,2007

5. Novel fibrinogen mutation gamma314Thr-->Pro (fibrinogen AI duPont) associated with hepatic fibrinogen storage disease and hypofibrinogenaemia;Brennan;Liver Int.,2010

Cited by 6 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. Guideline for diagnosis and management of congenital dysfibrinogenemia;Clinica Chimica Acta;2024-07

3. Two Novel Heterozygous Mutations (p.γPhe230Val and p.AαAsn839Thr) Cause Hereditary Hypodysfibrinogenemia in Two Chinese Independent Families;Acta Haematologica;2023

4. Congenital Fibrinogen Disorders, Diagnosis, and Management;Congenital Bleeding Disorders;2023

5. One Hundred Years of Congenital Fibrinogen Disorders;Seminars in Thrombosis and Hemostasis;2022-09-02

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