Research Article
A Chinese Family with Familial Dysalbuminemic Hyperthyroxinemia (FDH) due to R242H Mutation on Human Albumin Gene: Reevaluating the Role of FDH in Patients with Asymptomatic Hyperthyroxinemia
Figure 1
The pedigree of a Chinese family with familial dysalbuminemic hyperthyroxinemia (FDH).