View Labels for Central retinal artery occlusion associated with the G20210A prothrombin gene (F2) mutation: A case report.

• Central retinal artery occlusion associated with the G20210A prothrombin gene (F2) mutation: A case report.
• Oclusión de la arteria central de la retina asociado a la mutación del gen de la protrombina (F2) G20210A: un reporte de caso

English (United States)

• Central retinal artery occlusion associated with the G20210A prothrombin gene (F2) mutation: A case report.