| 1 | DUOX1, DUOXA1, HTDI3 |
| Identification of Two Missense Mutations in DUOX1 (p.R1307Q) and DUOXA1 (p.R56W) That Can Cause Congenital Hypothyroidism Through Impairing H2O2 Generation. | |
| Liu S, Han W, Zang Y, Zang H, Wang F, Jiang P, Wei H, Liu X, Wang Y, Ma X, Ge Y. | |
| Front Endocrinol (Lausanne) 10:526. doi: 10.3389/fendo.2019.00526. eCollection 2019. 2019 | |