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Article

Fibrinogen Montreal: a novel missense mutation (Aa D496N) associated with hypofibrinogenaemia.

Thrombosis and haemostasis - 1 Aug 2006

Sheen Campbell R, Brennan Stephen O, Jabado Nada, George Peter M

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 16894470

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.

Related research

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Fibrinogen Montreal: a novel missense mutation (Aa D496N) associated with hypofibrinogenaemia.PMID 16894470Read ↗

Fibrinogen Gdansk: hypofibrinogenemia associated with a novel missense mutation in FGA (Ser112Pro).Semantic proximity Read ↗

Fibrinogen Columbus III: A novel c.963del frameshift mutation in the FGG gene resulting in hypofibrinogenemia with a bleeding phenotype.Semantic proximity Read ↗

Fibrinogen Krakow: a novel hypo/dysfibrinogenemia mutation in fibrinogen gamma chain (Asn325Ile) affecting fibrin clot structure and function.Semantic proximity Read ↗

Novel fibrinogen Bbeta gene mutation causing hypofibrinogenaemia.Semantic proximity Read ↗

Hypofibrinogenaemia associated with novel Aα126Val→Asp mutation in the fibrinogen coiled coil.Semantic proximity Read ↗

Fibrinogen Nottingham II: a novel Bbeta Arg264gly substitution causing hypofibrinogenaemia.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 ↗

Fibrinogen Melbourne: a novel congenital hypodysfibrinogenemia caused by γ326Cys-Phe in the fibrinogen γ chain, presenting as massive splanchnic venous thrombosis.Semantic proximity Read ↗

Inherited abnormalities of fibrinogen: 10-year clinical experience of an Italian group.Semantic proximity Read ↗

Fibrinogen Otsu I:A gammaAsn319,Asp320 deletion dysfibrinogen identified in an asymptomatic pregnant woman.Semantic proximity Read ↗

Two novel mutations at contiguous codons in the fibrinogen Bbeta chain associated with hypofibrinogenaemia.Semantic proximity Read ↗

Fibrinogen Milano XIII (Aalpha 19 Arg-->Gly): a dysfunctional variant with an amino acid substitution in the N-terminal polymerization site.Semantic proximity Read ↗

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