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Article

Mutations in GPIIIa molecule as a cause for Glanzmann thrombasthenia in Indian patients.

Journal of thrombosis and haemostasis : JTH - 1 Mar 2005

Nair S, Ghosh K, Shetty S, Mohanty D

Abstract excerpt

BACKGROUND: Glanzmann thrombasthenia (GT) results from a quantitative or qualitative defect of GPIIb-IIIa complex, the fibrinogen receptor on platelets, which plays a very important role in platelet aggregation. In this report we describe the molecular studies on 22 patients with Glanzmann Thrombasthenia at our institute. OBJECTIVES: The main objective was to identify the mutations present in our GT population in...

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Identifiers

PMID: 15748237
DOI: 10.1111/j.1538-7836.2005.01159.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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