Mutations in the Iodotyrosine Deiodinase Gene and Hypothyroidism
J.C. Moreno(University of Amsterdam), Hans van Toor(Erasmus MC), Mariella D’Alessandro(University of Dundee), Annette Grüters(Humboldt-Universität zu Berlin), Michel Polak(Délégation Paris 5), Graziella Pinto(Hôpital Necker-Enfants Malades)
Cited by 196
Related Papers
Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans
|Nature Genetics|1998|1.7k
Autoantibodies against IL-17A, IL-17F, and IL-22 in patients with chronic mucocutaneous candidiasis and autoimmune polyendocrine syndrome type I
|The Journal of Experimental Medicine|2010|721
PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis
|Nature Genetics|1998|502
Inactivating Mutations in the Gene for Thyroid Oxidase 2 (<i>THOX2</i>) and Congenital Hypothyroidism
|New England Journal of Medicine|2002|477
Proopiomelanocortin Deficiency Treated with a Melanocortin-4 Receptor Agonist
|New England Journal of Medicine|2016|469