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Article

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

Thrombosis research - 1 Dec 1999

Bolliger-Stucki B, Bucciarelli P, Lämmle B, Furlan M

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Identifiers

PMID: 10605955
DOI: 10.1016/s0049-3848(99)00128-0

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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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Fibrinogen Milano XIII (Aalpha 19 Arg-->Gly): a dysfunctional variant with an amino acid substitution in the N-terminal polymerization site.PMID 10605955Read ↗

Fibrinogen Milano XII: a dysfunctional variant containing 2 amino acid substitutions, Aalpha R16C and gamma G165R.Semantic proximity Read ↗

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

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

A new substitution, gamma 358 Ser-->Cys, in fibrinogen Milano VII causes defective fibrin polymerization.Semantic proximity Read ↗

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

Human fibrinogen--structural variants and functional sites.Semantic proximity Read ↗

Fibrinogen Leipzig II (gamma351Gly-->Ser and gamma82Ala-->Gly): hypodysfibrinogenaemia due to two independent amino acid substitutions within the same polypeptide chain.Semantic proximity Read ↗

Fibrinogen anomalies and disease. A clinical update.Semantic proximity Read ↗

A frameshift mutation in Exon V of the A alpha-chain gene leading to truncated A alpha-chains in the homozygous dysfibrinogen Milano IIISemantic proximity Read ↗

Novel fibrinogen (B β401Gly→Val) presents as dys- or hypodysfibrinogenaemia due to alterations in sialic acid content.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 ↗

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

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