ArticleInternational journal of endocrinology2019

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.

Hongbing Liu et al.PubMed ↗Full text ↗Publisher ↗

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