Identification of PENDRIN (SLC26A4) mutations in patients with congenital hypothyroidism and “apparent” thyroid dysgenesis - Kühnen, P; Turan, S; Fröhler, S; Güran, T; Abali, S; Biebermann, H; Bereket, A; Grüters, A; Chen, W; Krude, H (J Clin Endocrinol Metab, 2014)