The Prothrombin Gene G20210A Mutation and the Platelet Glycoprotein IIIa Polymorphism PlA2 in Patients with Central Retinal Vein Occlusion
Author:
Publisher
Elsevier BV
Subject
Hematology
Reference27 articles.
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1. CENTRAL RETINAL VEIN OCCLUSION IN OTHERWISE HEALTHY CHILDREN AND ADOLESCENTS;Retina;2020-07
2. Genetic correlation between Prothrombin G20210A polymorphism and retinal vein occlusion risk;Brazilian Journal of Medical and Biological Research;2019
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4. Retinal vascular occlusion: a window to diagnosis of familial and acquired thrombophilia and hypofibrinolysis, with important ramifications for pregnancy outcomes;Clinical Ophthalmology;2016-08
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