Screening for mutations of the human thyroid peroxidase gene in patients with congenital hypothyroidism
Annette Grüters(Unknown), Heike Biebermann(Humboldt-Universität zu Berlin), Birgit Köhler(Linde (United States)), Ariane Söling, L. de Vijlder, Heiko Krude(Humboldt-Universität zu Berlin), Annika Wolf(Martin Luther University Halle-Wittenberg)
Cited by 24
Related Papers
Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans
|Nature Genetics|1998|1.7k
Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation
|The Lancet|2004|707
European Society for Paediatric Endocrinology Consensus Guidelines on Screening, Diagnosis, and Management of Congenital Hypothyroidism
|The Journal of Clinical Endocrinology & Metabolism|2014|569
PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis
|Nature Genetics|1998|503
Proopiomelanocortin Deficiency Treated with a Melanocortin-4 Receptor Agonist
|New England Journal of Medicine|2016|480