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

OBJECTIVE: Familial dysalbuminemic hyperthyroxinemia (FDH) has now become an established cause for spurious asymptomatic hyperthyroxinemia. Several different codon mutations on albumin gene had been identified. We here provided an established but rarely reported heterozygous mutation based on gene s...

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Detalles Bibliográficos
Autores principales: Liu, Hongbing, Ran, Jianmin, Chen, Chuping, Chen, Guangshu, Zhu, Ping, Tan, Rongshao, Liu, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6754905/
https://www.ncbi.nlm.nih.gov/pubmed/31582975
http://dx.doi.org/10.1155/2019/5947415

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6754905/
https://www.ncbi.nlm.nih.gov/pubmed/31582975
http://dx.doi.org/10.1155/2019/5947415

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