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Article

A deep vein thrombosis caused by 20209C>T mutation in homozygosis of the prothrombin gene in a Caucasian patient.

Biochemia medica - 1 Jan 2014

Alvarez Silvia Izquierdo, Ollero Eva Barrio, Llinares Sanjuan Francisco Miguel, Martínez Fabiola Lorente, Calvo Martín María Teresa

Abstract excerpt

INTRODUCTION: Additional nucleotide substitutions in the 3'-untranslated region of prothrombin gene could explain some thrombotic events and also adverse pregnancy outcomes. We describe the first case of a homozygous 20209C>T mutation as the cause of deep vein thrombosis in a Spanish patient. CASE AND METHODS: The 56-year-old male patient with a partial tear of the Achilles tendon developed calf (tibial) deep...

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Identifiers

PMID: 24627725
DOI: 10.11613/BM.2014.018
PMCID: PMC3936973

Genes

MTHFR
PTH

Provenance

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.

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