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Article

gammaAla82Gly represents a common fibrinogen gamma-chain variant in Caucasians.

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis - 1 Apr 2005

Ivaskevicius Vytautas, Jusciute Egle, Steffens Michael, Geisen Christof, Hanfland Peter, Wienker Thomas F, Seifried Erhard, Oldenburg Johannes

Abstract excerpt

Screening of 200 blood donors for the presence of polymorphisms in three fibrinogen genes (FGA, FGB, FGG), revealed two individuals with a heterozygous missense mutation (c.323C > G, gammaAla82Gly) in the FGG gene. This mutation has been reported previously to cause mild hypofibrinogenaemia. Analysis of an additional 416 blood donors showed two more heterozygous gammaAla82Gly mutations, resulting in an overall...

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Source

Identifiers

PMID: 15795540
DOI: 10.1097/01.mbc.0000164430.98169.c6

Genes

FGG
FGA
FGB

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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