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Article

A stop codon in a patient with severe type III von Willebrand disease.

Blood - 15 Aug 1991

Bahnak B R, Lavergne J M, Rothschild C, Meyer D

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PMID: 1868248

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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

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A stop codon in a patient with severe type III von Willebrand disease.PMID 1868248Read ↗

Identification of a new nonsense mutation in the von Willebrand factor gene in patients with von Willebrand disease type III.Semantic proximity Read ↗

Sense, missense, and nonsense: a novel mechanism of premature termination codon (PTC) mutation in a severe von Willebrand disease (VWD) patient.Semantic proximity Read ↗

Identification of a novel candidate splice site mutation (0874 + 1G > A) in a type 3 von Willebrand disease patient.Semantic proximity Read ↗

A G+3-to-T donor splice site mutation leads to skipping of exon 50 in von Willebrand factor mRNA.Semantic proximity Read ↗

A novel initiation codon mutation (ATG-->ATT) in a beta-thalassemia patient.Semantic proximity Read ↗

Nonsense mutations of the von Willebrand factor gene in patients with von Willebrand disease type III and type I.Semantic proximity Read ↗

An apparently silent nucleotide substitution (c.7056C>T) in the von Willebrand factor gene is responsible for type 1 von Willebrand disease.Semantic proximity Read ↗

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

Three missense mutations in Arg codons of the factor VIII genes of mild to moderately severe hemophilia A patients.Semantic proximity Read ↗

Molecular basis for hereditary antithrombin III quantitative deficiencies: a stop codon in exon IIIa and a frameshift in exon VI.Semantic proximity Read ↗

Errors in stop codon recognition in a temperature sensitive mutation of yeast.Semantic proximity Read ↗

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

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