MoranC, SegerC, TaylorK, OddyS, BurlingK, RajanayagamO, et al.2020. Hyperthyroxinemia and hypercortisolemia due to familial dysalbuminemia. Thyroid, 30:1681–1684.
2.
PannainS, FeldmanM, EiholzerU, WeissRE, ScherbergNH, RefetoffS. 2000. Familial dysalbuminemic hyperthyroxinemia in a Swiss family caused by a mutant albumin (R218P) shows an apparent discrepancy between serum concentration and affinity for thyroxine. J Clin Endocrinol Metab, 85:2786–2792.
3.
WadaN, ChibaH, ShimizuC, KijimaH, KuboM, KoikeT. 1997. A novel missense mutation in codon 218 of the albumin gene in a distinct phenotype of familial dysalbuminemic hyperthyroxinemia in a Japanese kindred. J Clin Endocrinol Metab, 82:3246–3250.
4.
HoshikawaS, MoriK, KaiseN, NakagawaY, ItoS, YoshidaK. 2004. Artifactually elevated serum-free thyroxine levels measured by equilibrium dialysis in a pregnant woman with familial dysalbuminemic hyperthyroxinemia. Thyroid, 14:155–160.
5.
PetitpasI, PetersenCE, HaCE, BhattacharyaAA, ZunszainPA, GhumanJ, et al.2003. Structural basis of albumin-thyroxine interactions and familial dysalbuminemic hyperthyroxinemia. Proc Natl Acad Sci U S A, 100:6440–6445.