A nonsense thyrotropin receptor gene mutation (R609X) is associated with congenital hypothyroidism and heart defects.


Cangul H., Bas V. N., Saglam Y., Kendall M., Barrett T., Maher E., ...More

Journal of pediatric endocrinology & metabolism : JPEM, vol.27, pp.1101-5, 2014 (SCI-Expanded) identifier identifier identifier