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Article

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

Haemophilia : the official journal of the World Federation of Hemophilia - 1 Nov 2015

Hua B, Li K, Lee A, Poon M-C, Zhao Y

Abstract excerpt

INTRODUCTION: Both congenital dysfibrinogenemia and haemophilia B (HB) are rare coagulopathies caused by mutations within the fibrinogen and F9 genes respectively. AIM: To investigate the pathogenesis of combined dysfibrinogenemia with HB in a family. METHODS: Coagulation assays, factor IX (FIX) activity (one-stage method), fibrinogen activity (Clauss method), antigen (immunoturbidimetry), fibrinogen...

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Source

Identifiers

PMID: 25982359
DOI: 10.1111/hae.12712

Genes

FGG

Variants

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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