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Article

Modulation of clinical phenotype of Glanzmann's thrombasthenia by thrombogenic mutations.

Clinica chimica acta; international journal of clinical chemistry - 1 May 2009

Kannan Meganathan, Yadav Birendra Kumar, Ahmad Firdos, Biswas Arijit, Saxena Renu

Abstract excerpt

BACKGROUND: Glanzmann's thrombasthenia (GT) is an autosomal recessive bleeding disorder which is due to a defect in platelet aggregation in response to multiple physiological agonists. It has been demonstrated that the clinical phenotype of various diseases inherited in a classic Mendelian fashion can be modulated by a series of factors, inherited as well as acquired. METHODS: A total of 45 GT patients were...

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Identifiers

PMID: 19245802
DOI: 10.1016/j.cca.2009.02.009

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MTHFR

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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