Ebrhim RS, Furman AE, Watanabe Y, Bruellman RJ, et al. Congenital Hypothyroidism in Two Sudanese Families harboring a novel Iodotyrosine deiodinase mutation (IYD R279C). Thyroid 2023 Jan 12. doi: 10.1089/thy.2022.0492.
PMID: 36633921