A truncating DUOX2 mutation (R434X) causes severe congenital hypothyroidism.


Cangul H., Aycan Z., Kendall M., Bas V. N. , Saglam Y., Barrett T., ...More

Journal of pediatric endocrinology & metabolism : JPEM, vol.27, pp.323-7, 2014 (Journal Indexed in SCI Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 27
  • Publication Date: 2014
  • Doi Number: 10.1515/jpem-2013-0314
  • Title of Journal : Journal of pediatric endocrinology & metabolism : JPEM
  • Page Numbers: pp.323-7