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Article

Hypofibrinogenaemia associated with common gamma82Ala-->Gly mutation is not mediated by altered mRNA splicing.

Thrombosis and haemostasis - 1 Oct 2006

Brennan Stephen O, Homer Vivienne M, Davis Ryan L, Meyer Michael, George Peter M

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 17003934

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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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Hypofibrinogenaemia associated with common gamma82Ala-->Gly mutation is not mediated by altered mRNA splicing.PMID 17003934Read ↗

gamma-Chain dysfibrinogenemias: molecular structure-function relationships of naturally occurring mutations in the gamma chain of human fibrinogen.Semantic proximity Read ↗

Hypofibrinogenemia in an individual with 2 coding (gamma82 A-->G and Bbeta235 P-->L) and 2 noncoding mutations.Semantic proximity Read ↗

Identification of a novel splicing mutation in the fibrinogen Aalpha chain gene leading to hypofibrinogenaemia in a Chinese pedigree.Semantic proximity Read ↗

Hypofibrinogenaemia with compound heterozygosity for two gamma chain mutations - gamma 82 Ala-->Gly and an intron two GT-->AT splice site mutation.Semantic proximity Read ↗

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gammaAla82Gly represents a common fibrinogen gamma-chain variant in Caucasians.Semantic proximity Read ↗

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Functionally compromised FGG variant (γ320Asp→Glu) expressed at low level in plasma fibrinogen.Semantic proximity Read ↗

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