José M. Miralles García

A new compound heterozygous for c.886C>T/c.2206C>T [p.R277X/p.Q717X] mutations in the thyroglobulin gene as a cause of foetal goitrous hypothyroidism

R. González-Sarmiento, Cintia E. Citterio, H. Targovnik, 2011, Clinical endocrinology.