[Clinical and genetic analysis of 8 Chinese pedigrees with inherited dysfibrinogenemia].
Jiang, Minghua; Wang, Xiaoou; Shu, Kuangyi; Jiang, Weiyan; Huang, Ying; Lin, Ying; Li, Shanshan; Hu, Yunliang.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 31(2): 134-9, 2014 Apr.
Artigo em Chinês | MEDLINE | ID: mdl-24711018
Human Fibrinogen: Molecular and Genetic Aspects of Congenital Disorders.
Nasledstvennaia afibrinogenemiia: obzor literatury i klinicheskie nabliudeniia.
[Analysis of a pedigree affected with congenital hypofibrinogenemia due to heterozygous Ser313Ile mutation of fibrinogen Î³ chain gene].
Clinical Consequences and Molecular Bases of Low Fibrinogen Levels.
A novel fibrinogen variant: dysfibrinogenemia associated with Î³Asp185Asn substitution.
Management of dysfibrinogenemia in pregnancy: A case report.
Laboratory and Genetic Investigation of Mutations Accounting for Congenital Fibrinogen Disorders.
Clinical features and molecular basis of 102 Chinese patients with congenital dysfibrinogenemia.
Thromboembolic events in patients with severe inherited fibrinogen deficiency.
Hepatic Fibrinogen Storage Disease in a Patient with Hypofibrinogenemia: Report of a Case with a Missense Mutation of the FGA Gene.