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Article

Inherited diseases of platelet glycoproteins: considerations for rapid molecular characterization.

Thrombosis and haemostasis - 1 Oct 1994

Bray P F

Abstract excerpt

The characterization of inherited diseases of platelets has provided valuable information about platelet physiology and platelet protein function. Genetic studies on patients with Glanzmann thrombasthenia, the Bernard-Soulier syndrome, and platelet-type von Willebrand disease have been confined to abnormalities of the GPIIb-IIIa and GPIb-IX receptor complexes. The primary molecular technique used in these...

Topics

Alleles
Bernard-Soulier Syndrome
Blood Platelet Disorders
DNA
DNA Mutational Analysis
False Negative Reactions
Genetic Techniques
Genotype
Humans
Platelet Membrane Glycoproteins
Polymerase Chain Reaction

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Polymorphism, Genetic

RNA, Messenger

Templates, Genetic

Thrombasthenia

Source

Identifiers

PMID: 7878622

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-7878622-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

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

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Inherited diseases of platelet glycoproteins: considerations for rapid molecular characterization.PMID 7878622Read ↗

Inherited platelet disorders.Semantic proximity Read ↗

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