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Article

Thrombophilic mutations and risk of retinal vein occlusion.

Arquivos brasileiros de oftalmologia - 1 Jan 2000

Biancardi Ana Luiza, Gadelha Telma, Borges Wander Inturias Sergillo, Vieira de Moraes Haroldo, Spector Nelson

Abstract excerpt

PURPOSE: The association of retinal vein occlusion and hereditary thrombophilia abnormalities is not established, with controversial results in the literature. This study investigates the association between retinal vein occlusion and three thrombophilic mutations: factor V 1691A (factor V Leiden), prothrombin 20210A (PT 20210A) and homozygous methylenetetrahydrofolate reductase 677T (MTHFR 677TT). METHODS: 55...

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Source

Identifiers

PMID: 18235909
DOI: 10.1590/s0004-27492007000600016

Genes

MTHFR

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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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