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Article

[Fibrinogen variation: a heterozygote dysfibrinogenemia with Arg-->His substitution in position 16 of the Aalpha chain].

Hamostaseologie - 1 May 2002

Seydewitz H H, Gram J, Bruhn H D, Witt I

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Share to Amino Acid Substitution
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 12193970

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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.

Related research

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Research trail→

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[Fibrinogen variation: a heterozygote dysfibrinogenemia with Arg-->His substitution in position 16 of the Aalpha chain].PMID 12193970Read ↗

[Genotype and function analyses of four inherited dysfibrinogenemia pedigree caused by Arg16 amino acid substitution in fibrinogen Aα chain].Semantic proximity Read ↗

[Inherited dysfibrinogenemia caused by Arg16His mutation in alpha chain of fibrinogen.].Semantic proximity Read ↗

Human Fibrinogen: Molecular and Genetic Aspects of Congenital DisordersSemantic proximity Read ↗

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

[Molecular variants of fibrinogen].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 ↗

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

[Phenotype and genotype analyses of two pedigrees with inherited fibrinogen deficiency].Semantic proximity Read ↗

Two different fibrinogen gene mutations associated with bleeding in the same family (A αGly13Glu and γGly16Ser) and their impact on fibrin clot properties: fibrinogen Krakow II and Krakow III.Semantic proximity Read ↗

[Inherited dysfibrinogenemia caused by Arg275His in the beta chain of fibrinogen].Semantic proximity Read ↗

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

[Research progress on hereditary fibrinogen abnormalities].Semantic proximity Read ↗

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