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 (SCI-Expanded) identifier identifier identifier