A Chinese Family with Familial Dysalbuminemic...

International Journal of Endocrinology 2019 / 09 Vol. 2019

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

Liu, Hongbing, Ran, Jianmin, Chen, Chuping, Chen, Guangshu, Zhu, Ping, Tan, Rongshao, Liu, Yan
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Volume:
2019
Journal:
International Journal of Endocrinology
DOI:
10.1155/2019/5947415
Date:
September, 2019
File:
PDF, 2.43 MB
2019
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