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.
Saved in:
| 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 |
|
Full text is not displayed to guests.
Login for full access.
|
|
| ISSN: | 01658107 |
|---|---|
| DOI: | 10.1080/01658107.2024.2402725 |