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Article

A second report of platelet-type von Willebrand disease with a Gly233Ser mutation in the GPIBA gene.

Thrombosis and haemostasis - 1 Feb 2007

Nurden Paquita, Lanza François, Bonnafous-Faurie Cécile, Nurden Alan

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

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Source

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PMID: 17264965

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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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A second report of platelet-type von Willebrand disease with a Gly233Ser mutation in the GPIBA gene.PMID 17264965Read ↗

Platelet-type von Willebrand disease: new insights into the molecular pathophysiology of a unique platelet defect.Semantic proximity Read ↗

Identification of p.W246L as a novel mutation in the GP1BA gene responsible for platelet-type von Willebrand disease.Semantic proximity Read ↗

Identification of a novel point mutation in platelet glycoprotein Ibalpha, Gly to Ser at residue 233, in a Japanese family with platelet-type von Willebrand disease.Semantic proximity Read ↗

A novel platelet-type von Willebrand disease mutation (GP1BA p.Met255Ile) associated with type 2B "Malmö/New York" von Willebrand disease.Semantic proximity Read ↗

A new heterozygous mutation in GP1BA gene responsible for macrothrombocytopenia.Semantic proximity Read ↗

A novel mutation in the GP1BA gene in Bernard-Soulier syndrome.Semantic proximity Read ↗

Gene of the issue: GP1BA gene mutations associated with bleeding.Semantic proximity Read ↗

Bernard–Soulier syndrome due to the homozygous Asn‐45Ser mutation in GPIX: an unexpected, frequent finding in GermanySemantic proximity Read ↗

A 10-base-pair deletion in the gene encoding platelet glycoprotein IIb associated with Glanzmann thrombasthenia in a horse.Semantic proximity Read ↗

Type IIB von Willebrand's disease: gene mutations and clinical presentation in nine families from Denmark, Germany and Sweden.Semantic proximity Read ↗

De novo mutation of the platelet glycoprotein Ib alpha gene in a patient with pseudo-von Willebrand disease.Semantic proximity Read ↗

An Arg545----Cys545 substitution mutation of the von Willebrand factor in type IIB von Willebrand's disease.Semantic proximity Read ↗

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