THE ROLE OF SLC26A4 MUTATIONS IN PENDRED SYNDROME: A GENETIC APPROACH TO HEARING AND THYROID DISORDERS. The Research of Medical Science Review, [S. l.], v. 2, n. 3, p. 637–652, 2024. Disponível em: http://thermsr.com/index.php/Journal/article/view/135.. Acesso em: 4 apr. 2025.