Coexisting congenital dysfibrinogenemia with a novel mutation in fibrinogen γ chain (γ322 Phe→Ile, Fibrinogen Beijing) and haemophilia B in a family.

Hua, B

Coexisting congenital dysfibrinogenemia with a novel mutation in fibrinogen γ chain (γ322 Phe→Ile, Fibrinogen Beijing) and haemophilia B in a family. [electronic resource] - Haemophilia : the official journal of the World Federation of Hemophilia Nov 2015 - 846-51 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

1365-2516

10.1111/hae.12712 doi


Adolescent
Afibrinogenemia--complications
Blood Coagulation Tests
DNA Mutational Analysis
Female
Fibrinogen--chemistry
Fibrinolysis
Hemophilia B--complications
Humans
Male
Mutation
Pedigree
Peptide Fragments--chemistry
Protein Multimerization
Protein Structure, Quaternary