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Article

Clinical and Molecular Study of Common Thrombophilia Mutation Prothrombin G20210A.

Advances in experimental medicine and biology - 1 Jan 2021

Angelopoulou Antonia, Vlachakis Dimitrios, Chrousos George P, Cosmidis Nikolaos, Yapijakis Christos

Abstract excerpt

BACKGROUND: One of the most common genetic causes associated with thrombophilia is mutation G20210A of the coagulation factor II (F2) gene. MATERIALS AND METHODS: Data collected from 355 unrelated Greeks examined for the mutation G20210A over a period of two decades were anonymously analyzed. RESULTS: The statistical analysis confirmed the importance of F2 G20210A in thrombosis and the significance of a positive...

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PMID: 35023122
DOI: 10.1007/978-3-030-78787-5_40

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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