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Article

Thrombophilic polymorphisms - factor V Leiden G1691A, prothrombin G20210A and MTHFR C677T - in Tunisian patients with cerebral venous thrombosis.

Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia - 1 Sept 2012

Ben Salem-Berrabah Olfa, Fekih-Mrissa Nejiba, N'siri Brahim, Ben Hamida Abdelmajid, Benammar-Elgaaied Amel, Gritli Nasreddine, Mrissa Ridha

Abstract excerpt

Cerebral venous thrombosis (CVT) has been associated with thrombophilic defects. We performed a study to evaluate the role of three single nucleotide polymorphisms (SNP), factor V Leiden G1691A (FVL), prothrombin gene mutation G20210A (FII-G20210A) and methylenotetrahydrofolate reductase variant...

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Source

Identifiers

PMID: 22721898
DOI: 10.1016/j.jocn.2011.11.029

Genes

MTHFR

Variants

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22721898-2026-09-04.1. Manifest publication-graph-cohort-2026-09-04.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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