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Article

Nonsense mutation Arg197stop in a Dutch family with type 1 hereditary antithrombin (AT) deficiency causing thrombophilia.

Thrombosis research - 1 May 1995

Michiels J J, van der Luit L, van Vliet H H, Jochmans K, Lissens W

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

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Identifiers

PMID: 7631305
DOI: 10.1016/0049-3848(95)90875-g

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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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Nonsense mutation Arg197stop in a Dutch family with type 1 hereditary antithrombin (AT) deficiency causing thrombophilia.PMID 7631305Read ↗

Novel point mutations leading to type 1 antithrombin deficiency and thrombosis.Semantic proximity Read ↗

A common point mutation producing type 1A antithrombin III deficiency: AT129 CGA to TGA (Arg to Stop).Semantic proximity Read ↗

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Recurrent ischemic cerebrovascular events in a patient with type I antithrombin deficiency caused by 9788 G>A splice site mutation: a case report.Semantic proximity Read ↗

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A novel missense mutation in the antithrombin III gene (Ala387-->Val) causing recurrent venous thrombosis.Semantic proximity Read ↗

Antithrombin III Budapest: a single amino acid substitution (429Pro to Leu) in a region highly conserved in the serpin family.Semantic proximity Read ↗

Two new nonsense mutations in type Ia antithrombin III deficiency at Leu 140 and Arg 197.Semantic proximity Read ↗

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