/
J Clin Endocrinol Metab
Identification of PENDRIN (SLC26A4) mutations in patients with congenital hypothyroidism and "apparent" thyroid dysgenesis
- P. Kuehnen
- S. Turan
- S. Froehler
- T. Gueran
- S. Abali
- H. Biebermann
- A. Bereket
- A. Grueters
- W. Chen
- H. Krude