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Clinical features and molecular basis of 102 Chinese patients with congenital dysfibrinogenemia

  • Published:2015-12 Issue:4 Volume:55 Page:308-315
  • ISSN:1079-9796
  • Container-title:Blood Cells, Molecules, and Diseases
  • language:en
  • Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Zhou Jingyi,Ding Qiulan,Chen Yaopeng,Ouyang Qi,Jiang Linlin,Dai Jing,Lu Yeling,Wu Xi,Liang Qian,Wang Hongli,Wang Xuefeng

Funder

National Basic Research Program of China

General Program of National Natural Science Foundation of China

Doctoral Innovation Fund Projects from Shanghai Jiaotong University School of Medicine

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference31 articles.

1. The structure and biological features of fibrinogen and fibrin;Mosesson;Ann. N. Y. Acad. Sci.,2001

2. Fibrinogen and fibrin structure and functions;Mosesson;J. Thromb. Haemost.,2005

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

4. A database for human fibrinogen variants;Hanss;Ann. N. Y. Acad. Sci.,2001

5. Clinical phenotype, laboratory features and genotype of 35 patients with heritable dysfibrinogenaemia;Shapiro;Br. J. Haematol.,2013

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