Acar S, Gursoy S, Arslan G, Nalbantoglu O, et al. Screening of 23 candidate genes by next-generation sequencing of patients with
permanent congenital hypothyroidism: novel variants in TG, TSHR, DUOX2, FOXE1,
and SLC26A7. J Endocrinol Invest 2021 Nov 15. pii: 10.1007/s40618-021-01706.
PMID: 34780050