[1]
“THE ROLE OF SLC26A4 MUTATIONS IN PENDRED SYNDROME: A GENETIC APPROACH TO HEARING AND THYROID DISORDERS”, RMSR, vol. 2, no. 3, pp. 637–652, Nov. 2024, Accessed: Nov. 21, 2024. [Online]. Available: https://thermsr.com/index.php/Journal/article/view/135