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Article

[Clinical and genetic aspects of antithrombin III deficiency and abnormal antithrombin III].

[Rinsho ketsueki] The Japanese journal of clinical hematology - 1 May 1991

Tsuji H

Abstract excerpt

Antithrombin III (AT III) has been confirmed to play an important role as a serine protease inhibitor in the mechanism of blood coagulation, and its deficiency or abnormality is found to cause thromboembolic disorders by reducing the anticoagulant activity. In this paper AT III gene of patient with congenital AT III deficiency, which was suggested to have qualitative abnormality by isoelectric focusing, was...

Topics

Antithrombin III
Antithrombin III Deficiency
Blotting, Southern
Electrophoresis, Agar Gel
Female
Humans
Male
Mutation
Phosphorus Radioisotopes

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 1870264

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-1870264-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

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[Clinical and genetic aspects of antithrombin III deficiency and abnormal antithrombin III].PMID 1870264Read ↗

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Congenital antithrombin III deficiency (AT-III Kyoto): identification of a point mutation altering arginine-406 to methionine behind the reactive site.Semantic proximity Read ↗

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