The Role of FOXP3 Polymorphisms in Graves' Disease with or without Ophthalmopathy in a Turkish Population.
Fulya Yaylacıoğlu TuncayKübra Serbest CeylanoğluSezen Güntekin ErgünGüntekin ErgünOnur KonukPublished in: Turkish journal of ophthalmology (2024)
The AC and AA genotypes of rs3761548 (-3279) and CT genotype of rs3761549 (-2383 C/T) were shown to be possible risk factors for GD development in the Turkish population. However, none of the three SNPs was shown to be associated with the development of GO in patients with GD.