Compound Heterozygosity for the C6777T Mutation of the MTHFR Gene and the FII G20210A Mutation of the Prothrombin Gene in Sequential Bilateral Anterior Ischemic Optic Neuropathy.

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Title: Compound Heterozygosity for the C6777T Mutation of the MTHFR Gene and the FII G20210A Mutation of the Prothrombin Gene in Sequential Bilateral Anterior Ischemic Optic Neuropathy.
Authors: Tsiogka, Anastasia1 (AUTHOR) anastasia.tsioga@gmail.com, Vlachos, Georgios1 (AUTHOR), Galanopoulos, Athanasios2 (AUTHOR), Rotsos, Tryfon1 (AUTHOR), Kandarakis, Stylianos1 (AUTHOR), Nikolopoulou, Anthi3 (AUTHOR), Karmiris, Efthymios1,4 (AUTHOR), Chatzistefanou, Klio I.1,3 (AUTHOR)
Source: Neuro-Ophthalmology. Jun2025, Vol. 49 Issue 3, p193-199. 7p.
Database: Academic Search Ultimate
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ISSN:01658107
DOI:10.1080/01658107.2024.2402725