Study of Deiodinase Type 2 Polymorphisms in Graves ’ Disease and Ophthalmopathy in a Swedish Population

Conclusions: Rs225011 in DIO2 was weakly associated with GD. The mechanism behind this association requires further study. None of the investigated common SNPs in DIO2 was significantly associated with GO, fT3, fT4, TRAb, or TPOAb in GD patients.Eur Thyroid J
Source: European Thyroid Journal - Category: Endocrinology Source Type: research