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 (Journal Indexed in SCI Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 27
  • Publication Date: 2014
  • Doi Number: 10.1515/jpem-2014-0025
  • Title of Journal : Journal of pediatric endocrinology & metabolism : JPEM
  • Page Numbers: pp.1101-5